Genex Pharma

Dose/Strength	100 mg
Strength	100 mg
Brand	Duron-100
Treatment	Cardiac Arrhythmias
Manufacturer	Samarth Life Science Pvt. Ltd.
Packaging Size	10*10 Tablets
Shelf Life	24 months
Packaging Type	Stripe
Country of Origin	Made in India

Product Name: Amiodarone Tablets
Brand Name: Duron
Strength: 100 MG
Packing:100 Tablets Per Box

Description:Amiodarone, an antiarrhythmics produces its helpful effects by slowing heart nerve impulses and acting directly on the heart tissues.

Indications: Amiodarone is an effective agent for the management of supraventricular and ventricular arrhythmias. It is indicated in controlling both atrial and ventricular arrhythmias associated with hypertrophic cardiomyopathy and may reduce the incidence of sudden death in these patients. DURON has been reported to improve mortality rates in patients surviving myocardial infarction.

Storage: Store at a temperature below 25°C. Protect from light and moisture.

Presentation: A box containing 6 blisters of 10 tablets each of Amiodarone HCl 100 mg 

Additional Information:

• Packaging Details: 100 TABLETS PER BOX

Route Of Administration	Intravenous
Brand	CARNOSIN
Container Type	Vial
Indication	Cardiovascular Disorders
Strength	6mg/1ml
Packaging Volume	2 ml
Dose	6MG/2ML
Injection Site	Intravenous
Packaging Size	Single Ampoule Per Box
Packaging Type	SINGLE AMPOULE PER BOX
Country of Origin	Made in India

<sub>Product Name: Adenosin Injection
Brand Name:Carnosin
Strength:6MG/ 2 ML
Packing:Single Ampoule Per Box

Description: Adenosine is a purine nucleoside that forms from the breakdown of adenosine triphosphate (ATP). ATP is the primary energy source in cells for transport systems and many enzymes.</sub>Indication: CARNOSIN is indicated for the following:

_{Treatment of Paroxysmal Supraventricular tachycardia(PSVT).
Diagnosis of re-entrant atrial and ventracular tachycardia.
Non-invasive assessment of coronary artery disease(CAD) using techniques like pharmaco logical stress testing, single photon emission computed tomography(SPECT), thallium-201 scintigraphy and positron emission tomography.
Storage: Store at temperature not exceeding 25°C. Protect from light. Do not freeze.
Presentation: Adenosine Injection USP is available as 2 ml ampoule, individually-boxed.} 

 

Strength	0.25 mg
Brand	Dixin
Manufacturer	Samarth Life Science Pvt Ltd
Pack Type	Box
Shelf Life	18 month
Storage	Below 25°C
Packaging Type	200 Tablets per box
Brand Name	Dixin
Grade Standard	Medicine Grade
Pack Size	10*20 Tablet
Country of Origin	Made in India

Product Name: Digoxin Tablets
Brand Name: Dixin
Strength: 25 MG
Packing: 200 Tablets Per Box

Product Description

Digoxin Tablets (Dixin) 0.25 mg are a cardiac glycoside formulation developed by Genex Pharma to support the management of various cardiovascular conditions. Derived from the leaves of the Digitalis plant, digoxin has been widely used for decades in treating heart rhythm disorders and heart failure. By improving myocardial contractility and controlling heart rate, Digoxin (Dixin) plays a critical role in restoring cardiac efficiency and improving quality of life for patients with compromised heart function.

Composition

• Active Ingredient: Digoxin 0.25 mg per tablet

• Excipients: Pharmaceutical grade inactive ingredients to ensure stability, safety, and effectiveness

Indications

Digoxin Tablets (Dixin) 0.25 mg are indicated for:

• Heart Failure: Improving symptoms in patients with reduced ejection fraction (systolic heart failure) by enhancing cardiac output.

• Atrial Fibrillation (AF): Controlling ventricular response in atrial fibrillation and atrial flutter.

• Atrial Tachyarrhythmias: Management of certain supraventricular arrhythmias where slowing the ventricular rate is required.

Storage

• Store below 25°C in a cool, dry place

• Protect from light and moisture

• Keep out of reach of children

Additional Information:

• Delivery Time: 4-5 WEEKS
• Packaging Details: 200 TABLETS PER BOX

Patient Type	Adult
Set Configuration	Single Line
Usage Type	Single Use
Usage/Application	Hospital
Tubing Material	Silicone
Type	Surgical Equipments
Max Flow Rate	200 ml/min
Filter Pore Size	20 micron
Brand	PLEGIOCARD
Country of Origin	Made in India
Packing	20 Ampoules Per Box

Product Name: Cardioplegia Solution
Brand Name: Plegiocard
Strength: 20 ML
Packing: 20 Ampoules Per Box

1. Purpose: Induces temporary cardiac arrest during open-heart surgery, allowing surgeons to operate on the heart while it is still and bloodless.

2. Composition: Typically contains potassium chloride to stop the heart's electrical activity and protect it from damage during surgery.

3. Mechanism of Action: Works by depolarizing cardiac cells, halting heart contractions, and preventing muscle damage during surgery.

4. Administration: Administered directly into the coronary arteries or into the heart chambers by the surgical team.

5. Dosage: Dosage is carefully calculated based on the patient's weight, cardiac condition, and surgical requirements.

6. Monitoring: Continuous monitoring of cardiac function, electrolyte levels, and vital signs is essential during administration to ensure the heart remains stable.

7. Adverse Effects: Potential side effects include arrhythmias, electrolyte imbalances, and myocardial dysfunction.

8. Contraindications: Should not be used in patients with severe electrolyte abnormalities or those with hypersensitivity to its components.

9. Storage: Store in a cool, dry place at controlled room temperature. Protect from light and moisture.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: 20 Ampoules Per Box

Strength	20 MG
Packaging Size	20mg/4ml
Vial Volume	4 ml
With Dextrose	With Dextrose
Container Type	Glass Bottle
Route	Infiltration
Brand	Numbcaine
Pack Size	4ML
Manufacture By	Samarth Life Science Pvt. Ltd.
Pack	BOX
Country of Origin	Made in India
Packaging Type	Vial
Pack Type	Ampoule

Product Name: Bupivacaine HCL In Dextrose Injection 20 MG/ 4 ML
Strength: 20 MG/ 4 ML
Brand Name: Numcaine Heavy
Packing: 5 Ampoules Per Box

Description: Bupivacaine hydrochloride is 1-Butyl-26-pipecoloxylidide monochloride monohydrate. Bupivacaine Heavy (Bupivacaine in Dextrose Injection, USP) is sterile, hyperbaric solution for subarachnoid injection (Heavy block).

Indication: Bupivacaine Heavy is indicated for the production of subarachnoid block (Heavy anesthesia).

Storage: Store in a cool dry place. Protect from light. Presentation: 5 Ampoules of 4mL per Box.
Drug Composition: Bupivacaine hydrochloride, a local anesthetic, in dextrose solution

Primary Use: Provides local anesthesia for surgical procedures, obstetrical analgesia, and pain management

Administration: Typically administered via epidural or spinal injection

Mechanism of Action: Blocks nerve impulses by inhibiting sodium ion influx through nerve cell membranes

Dosage: Administered based on the specific procedure and patient factors, with careful attention to maximum recommended doses

Onset of Action: Rapid onset of anesthesia within minutes

Duration of Action: Prolonged duration of anesthesia, lasting several hours

Side Effects: Common side effects include hypotension, bradycardia, and potential
neurologic complications such as numbness or weakness; systemic toxicity can occur with high doses

Contraindications: Hypersensitivity to bupivacaine or amide-type local anesthetics, severe cardiovascular disease, or certain neurological conditions

Monitoring: Continuous monitoring of vital signs and neurological status during administration, with readiness to manage potential complications

Drug Interactions: Potential interactions with other medications affecting cardiovascular or neurological function

Special Precautions: Use with caution in patients with impaired cardiovascular function or neurological disorders; avoid intravascular injection to minimize systemic toxicity risks

Patient Education: Inform patients about expected effects, potential risks, and the importance of reporting any unusual symptoms promptly to healthcare providers.

Additional Information:

• Packaging Details: 5 AMPOULES PER BOX

Strength	500 mcg
Brand	ALPOSTIN
Pack Size	SINGLE AMPOULE PER BOX
Form	Injection
Composition	Alprostadil
Route Of Administration	Intraurethral
Packaging Type	Box
Manufacturer	SAMARTH LIFESCIENCES PVT LTD

Product Name: Alprostadil (Prostaglandin E1) Injection
Brand Name: Alpostin
Strength:500 MCG/ 1 ML 
Packing: Single Ampoule Per Box

We are Genex Pharma, a reputable Indian pharmaceutical manufacturer and global exporter, offers Alpostin for international markets, hospital tenders, institutional procurement, and contract manufacturing. With a strong focus on quality, regulatory compliance, and cold chain logistics, Genex Pharma delivers timely exports and provides customizable packaging solutions tailored to specific country requirements.

Alprostadil Injection, USP for intravascular infusion contains 500 micrograms alprostadil, more commonly known as prostaglandin E1, in 1 mL dehydrated alcohol.
Composition Each ml contains : Alprostadil USP 500mcg Absolute Alcohol IP q.s.
Clinical Pharmacology : Alprostadil (prostaglandin E1) is one of a family of naturally occurring acidic lipids with various pharmacologic effects. Vasodilation, inhibition of platelet aggregtion, and stimulation of intestinal and uterine smooth muscle are among the most notable of these effects. Intravenous doses of 1 to 10 micrograms of alprostadil per kilogram of body weight lower the blood pressure in mammals by decreasing peripheral resistance. Reflex increases in cardiac output and rate accompany reduction in blood pressure. the Smooth muscle of the ductus arteriosus is especially sensitive to alprostadil, and strips of lamb ductus markedly relax in the presence of the drug. In addition, administration of alprostadil reopened the closing ductus of new-born rats, rabbits, and lambs. These observations led to the investigation of alprostadil in infants who had congenital defects which restricted the pulmonary or systemic blood flow and who depended onapatent ductus arteriosus for adequate blood oxygenation and lower body perfusion.
Indication and Usage: Alprostadil injection is indicated for palliative, not definitive, therapy to temporarily maintain the patency of the ductus arteriosus until corrective or palliative surgery can be performed in neonates who have congenital heart defects and who depend upon the patent ductus for survival. Such congenital heart defects include pulmonary atresia, pulmonary stenosis, tricuspid atresia, tetralogy of Fallot, interruption of the aortic arch, coarctation of the aorta, or transposition of the great vessels with or without other defects.
Dosage and Administration: The preferred route of administration for alprostadil injection is continuous intravenous infusion into a large vein. Alternatively, alprostadil injection may be administered through an umbilical artery catheter placed at the ductal opening.
Storage: Store at a temperature between 2° and 8° C. Protect from light.

Strength	100 mcg
Brand	Samarth
Packaging Size	1 ml
Usage/Application	Commercial
Packaging Type	Vial
Composition	Dexmedetomidine Hydrochloride
Manufacturer	Samarth Life Science Pvt. Ltd.
Form	Injection
Country of Origin	Made in India

Product Name: Dexmedetomidine Hydrochloride Injection
Brand Name: Dexmedine
Strength: 100 MG/ 1 ML
Packing: Single Ampoule Per Box

• Active Ingredient: Dexmedetomidine hydrochloride
• Strength: Available in various strengths, typically 100 mcg/mL or 200 mcg/2 mL (concentration may vary by manufacturer)
• Form: Injectable solution
• Administration Route: Intravenous (IV) infusion
• Indication: Sedation of initially intubated and mechanically ventilated patients in the intensive care unit (ICU); procedural sedation for non-intubated patients
• Mechanism of Action: Alpha-2 adrenergic agonist; provides sedative, anxiolytic, and analgesic effects by inhibiting norepinephrine release
• Dosage: Dosage and infusion rate depend on the desired level of sedation and patient response; often started with a loading dose followed by maintenance infusion
• Side Effects: Hypotension, bradycardia, dry mouth, nausea, fever, hypertension, atrial fibrillation
• Contraindications: Hypersensitivity to dexmedetomidine or any component of the formulation
• Precautions: Monitor blood pressure, heart rate, and oxygenation during treatment; use with caution in patients with advanced heart block or severe ventricular dysfunction
• Storage: Store at controlled room temperature (20-25°C); protect from light

Additional Information:

• Packaging Details: Single Ampoule Per Box

Strength	50 mcg
Brand	DEXMEDINE
Packaging Size	0.5 ml
Packaging Type	Ampoule
Usage/Application	Procedural Sedation
Also Gives	PCD Pharma Franchise
Brand Name	Dexmedine

Product Name: Dexmedetomidine Hydrochloride Injection
Brand Name: Dexmedine
Strength: 50 MCG/0.5 ML
Packing: Single Ampoule Per Box

Dexmedetomidine Hydrochloride Injection, 50 MCG, is a potent medication used for sedation and pain management in medical procedures and critical care. Administered by healthcare professionals, it acts on brain receptors to induce sedation, relieve pain, and reduce anxiety. This injection is commonly used for conscious sedation in procedures like mechanical ventilation and minor surgeries, allowing patients to stay cooperative and easily awakened. It provides a safer alternative to other sedatives, with minimal impact on breathing and heart function.

Strength	200 mcg
Brand	samarth
Packaging Size	2 ml
Usage/Application	Hospital
Packaging Type	Ampoule
Composition	Dexmedetomidine Hydrochloride
Also Gives	PCD Pharma Franchise
Country of Origin	Made in India

Product Name: Dexmedetomidine Hydrochloride Injection
Brand Name: Dexmedine
Strength: 200 MG/2 ML
Packing: Single Ampoule Per Box

• Active Ingredient: Dexmedetomidine hydrochloride
• Strength: Available in various strengths, typically 100 mcg/mL or 200 mcg/2 mL (concentration may vary by manufacturer)
• Form: Injectable solution
• Administration Route: Intravenous (IV) infusion
• Indication: Sedation of initially intubated and mechanically ventilated patients in the intensive care unit (ICU); procedural sedation for non-intubated patients
• Mechanism of Action: Alpha-2 adrenergic agonist; provides sedative, anxiolytic, and analgesic effects by inhibiting norepinephrine release
• Dosage: Dosage and infusion rate depend on the desired level of sedation and patient response; often started with a loading dose followed by maintenance infusion
• Side Effects: Hypotension, bradycardia, dry mouth, nausea, fever, hypertension, atrial fibrillation
• Contraindications: Hypersensitivity to dexmedetomidine or any component of the formulation
• Precautions: Monitor blood pressure, heart rate, and oxygenation during treatment; use with caution in patients with advanced heart block or severe ventricular dysfunction
• Storage: Store at controlled room temperature (20-25°C); protect from light

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 Weeks
• Packaging Details: Single Ampoule Per Box

Physical Form	Lyophilized
Packaging Type	Vial
Route Of Administration	Intravenous
Packaging Size	SINGLE VIAL PER BOX
Brand	Levosimed
Treatment	Cardiac Surgery
Manufacturer	SAMARTH LIFESCIENCES
Usage/Application	Hospital
Prescription/Non prescription	Prescription
Strength	12.5 mg

Product Name: Levosimendan for Injection 12.5 mg
Brand Name: Levosimed
Strength: 12.5 mg
Packing: 1 Vial

Levosimendan for Injection 12.5 mg is a medication primarily used in the management of acute heart failure and inotropic support during cardiac surgery. Here's a concise overview of its key features:

• Medical Use: Levosimendan for Injection 12.5 mg is administered to improve cardiac contractility and enhance cardiac output in acute heart failure situations.

• Mechanism of Action: It works by sensitizing cardiac myofilaments to calcium, leading to enhanced cardiac contractility without increasing myocardial oxygen consumption.

• Dosage Strength: Each vial contains 12.5 mg of Levosimendan, providing a standardized dose for intravenous administration.

• Onset of Action: Rapid onset of action makes it suitable for acute situations where immediate cardiac support is required.

• Medical Supervision: Administration should be under close supervision of healthcare professionals experienced in the management of acute heart failure due to the potential for significant hemodynamic effects.

• Side Effects: Common side effects may include hypotension, arrhythmias, and headache. Careful monitoring is necessary to mitigate potential adverse reactions.

• Contraindications: Avoid in patients with severe hypotension, severe renal impairment, or those receiving concomitant strong CYP3A4 inhibitors.

• Storage: Store in a cool, dry place, away from sunlight and out of reach of children, following manufacturer's instructions to maintain efficacy and safety.

Levosimendan for Injection 12.5 mg serves as a valuable intervention in acute heart failure, providing rapid and effective support to optimize cardiac function in critical situations.

Additional Information:

• Packaging Details: SINGLE VIAL PER BOX

Concentration	99.9%
Strength	1 mg
Pack Volume	30ML
Bottle Type	Clear Glass
Usage	muscle relaxation and reduces pains
Packaging Type	Vial
Grade	IP
Packaging Size	30ml
Brand	Isoflurane
Storage	15-30 DegreeC
Shelf life	2 Years
Also Gives	PCD Pharma Franchise
Prescription/Non-Prescription	Prescription
Country of Origin	Made in India
Stability	Isoflurane is chemically stable under normal storage conditions, but exposure to extreme temperature
Opened Containers	Once opened, use the product as soon as possible, although specific recommendations for open vial us

Product Name: Isoflurane Liquid for Inhalation
Brand Name: Iflurane-30
Strength: 30 ML
Packing:Single Bottle Per Box

• Isoflurane Liquid For Inhalation 30 ML is an inhalation anesthetic used to induce and maintain general anesthesia during surgical procedures.
• It is administered through a specialized vaporizer and delivered to the patient via inhalation.
• Isoflurane belongs to the class of halogenated ethers and works by depressing the central nervous system to produce anesthesia.
• This liquid formulation comes in a 30 milliliter container and is vaporized to a gas form before inhalation.
• Isoflurane is commonly used due to its rapid onset and offset of action, allowing for precise control of anesthesia depth.
• Dosage and administration should be carefully monitored by trained anesthesia professionals to ensure patient safety and optimal anesthesia depth.
• Side effects may include respiratory depression, hypotension, and postoperative nausea and vomiting.
• Isoflurane is stored and handled with caution as it is a flammable liquid and should be kept away from heat sources.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 3-4 Weeks
• Packaging Details: SINGLE BOTTLE PER BOX

Brand	FOXIFUSE
Pack Size	20 ml Vial
Strength	500mg/10ml
Packaging Type	Single Vial Per Box
Usage	Iron Deficiency
Packaging size	1 G /20 ML ( 50 MG/ML)
Brand Name	Foxifuse
Manufacturer	Samarth Life Science Pvt. Ltd
Country of Origin	Made in India

Product Name:Ferric Carboxymaltose Injection
Brand Name: Foxifuse
Strength: 1 G/ 20 ML ( 50 MG/ML)
Packing: Single Vial Per Box

Description:
Foxifuse is a high-dose intravenous iron formulation containing Ferric Carboxymaltose equivalent to 1,000 mg elemental iron in 20 mL. It is designed to rapidly replenish iron stores in patients with iron deficiency or iron deficiency anemia, particularly when oral iron is ineffective, poorly tolerated, or contraindicated.

Composition:

• Each 20 mL vial contains:
  Ferric Carboxymaltose 1,000 mg (as elemental iron)

Storage:

• Store below 25°C.

• Do not freeze.

• Protect from light.

Packaging:

• Vial of 20 mL containing 1,000 mg of elemental iron.

• Sterile, single-use vial.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 WEEKS
• Packaging Details: Single Vial Per Box

Strength	300 mg/3 ml
Brand	ZeroklotPen
Form	Injection
Pack Type	Vial
Volume	3 ml
Salt Type	Enoxaparin sodium
Pack Size	1 syringe
Brand Name	Zerokot
Manufacturer	Samarth Science Pvt. Ltd
Usages	for preventing and treating blood clots.
Prescription/ Non Prescription	Prescription
Packaging Type	Pre filled syringe
Also Gives	Pharmaceutical Third Party Manufacturing
Country of Origin	Made in India
Composition	Enoxaparin Sodium 300mg / Excipients
Packing	SINGLE PEN PER BOX
Strengths	300 mg / 3ml

Product Name: Enoxaparin Injection 
Brand Name: Zeroklot
Strength:300 MG/ 3ML
Packing:Single Pen Per Box

Enoxaparin Injection 300 mg/3 mL by Genex Pharma is a low molecular weight heparin (LMWH) used for preventing and treating blood clots. It is indicated for DVT and PE prevention, acute coronary syndrome (ACS), thrombosis management in dialysis patients, and post-surgical clot prevention.
Enoxaparin Injection is a low molecular weight heparin (LMWH) used as an anticoagulant to prevent and treat blood clots. It is derived from unfractionated heparin and provides enhanced antithrombotic activity with a reduced risk of bleeding compared to standard heparins.

Composition

Each 3 mL prefilled syringe contains:

• Enoxaparin Sodium – 300 mg (equivalent to 100 mg/mL)
• Excipients – Water for Injection, Sodium Hydroxide (for pH adjustment)

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE PEN PER BOX

Strength	40 mg
Brand	Lowcap
Form	Prefilled Syringe
Pack Type	Vial
Volume	0.4 ml
Salt Type	Enoxaparin sodium
Pack Size	0.4 ml
Brand Name	Lowcap
Manufacturer	Samarth
Packaging Type	Pre filled syringe
Country of Origin	Made in India
Dose Strength	40 mg/0.4 ml
Packing Type	Single PFS per Box

Enoxaparin Sodium Injection (LOWCAP 40 mg / 0.4 mL)

1. Brand Name: LOWCAP 
2. Composition: Enoxaparin Sodium 40 mg / 0.4 mL
3. Form: Prefilled Syringe (Single-use)
4. Therapeutic Use: Anticoagulant for prevention and treatment of blood clots
5. Mechanism of Action: Enoxaparin is a low molecular weight heparin (LMWH) that inhibits clot formation by enhancing the activity of antithrombin III, leading to the inhibition of factor Xa and thrombin.
6. Indications:
   • Prevention of deep vein thrombosis (DVT) and pulmonary embolism (PE) in patients undergoing surgery
   • Treatment of acute deep vein thrombosis (DVT) and pulmonary embolism (PE)
   • Prevention of ischemic complications in patients with unstable angina and non-Q-wave myocardial infarction
7. Dosage: As prescribed by the physician, typically administered subcutaneously.
8. Packaging: 1 prefilled syringe (Single-use) per box
9. Shelf Life: 24 months from manufacturing date
10. Storage Conditions: Store below 25°C, protect from light and moisture.
11. Key Features:

• Convenient prefilled syringe for easy administration
• Safe for use in patients requiring anticoagulation therapy
• Ideal for both hospital and outpatient use

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 Weeks
• Packaging Details: A Single Vial Per Box

Strength	100 mg
Dose/Strength	100 mg
Pack Size	5 x 10 tablets
Pharmacopeia Standard	IP
Usage / Application	Clinical
Brand	Eubet
Manufacturer	SAMARTH LIFE SCIENCES PVT LTD.
Dosage	100MG
Generic	LABETALOL TABLETS

Product :Labetalol Tablets
Brand Name: Eubet
Strength:100 MG
Packing: 50 Tablets Per Box
_{Product Description:}EUBET 100 mg is an oral antihypertensive medication containing Labetalol, a unique non-selective beta-blocker with selective alpha-1 blocking activity. This dual mechanism makes it effective in reducing blood pressure without significantly lowering heart rate or cardiac output. EUBET is used in the management of mild to moderate hypertension, including in pregnant women with preeclampsia, and is also useful in treating hypertensive emergencies under medical supervision. _Indications:

EUBET (Labetalol 100 mg Tablets) is indicated for the treatment of:
Mild to moderate hypertension
Hypertensive crisis or emergencies (oral continuation after parenteral therapy)
Hypertension in pregnancy, including preeclampsia
Refractory hypertension as part of combination therapy

 

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: 50 TABLETS PER BOX

Strength	250 mg
Pack Size	5 ml
Brand	Samarth Life Science Pvt Ltd
Pack Type	Vial
Composition	Dobutamine
Form	Injection
Packaging Type	Single vial per box.
Brand Name	Dobustat
Manufactured By	Samarth Lifesciences
Grade Standard	Medicine Grade
Country of Origin	Made in India

Product Name: Dobutamine HCL Injection
Brand Name:Dobustat
Strength: 250 MG/5 ML
Packing: 2 Ampoules Per Box

_{Product Description}Dobustat (Dobutamine HCl Injection) 250 mg/5 mL by Genex Pharma is a sterile, clear solution for intravenous use, formulated to provide rapid and effective inotropic support in patients with acute cardiac decompensation. Dobutamine, a synthetic catecholamine, acts directly on β1-adrenergic receptors of the heart, enhancing myocardial contractility and stroke volume without significantly increasing heart rate or myocardial oxygen demand.

^Indications

Dobustat is indicated for:

• Short-term treatment of cardiac decompensation due to depressed contractility from organic heart disease or following cardiac surgery.

• Management of cardiogenic shock secondary to myocardial infarction, cardiac surgery, or septic/cardiomyopathic shock.

• Low cardiac output states where inotropic support is required.

 

 

Brand	FOXIFUSE
Pack Size	10 ml Vial
Packaging Type	Single Vial Per Box
Usage	Iron Deficiency
Packaging size	10 ML
Brand Name	Foxifuse
Manufacturer	Samarth Life Science Pvt. Ltd.
Country of Origin	Made in India
Strength	750 mg

Product Name: Ferric Carboxymaltose Injection
Brand Name: Foxifuse
Strength: 500 MG/ 10 ML
Packing: Single Vial Per Box

Description:
Foxifuse (Ferric Carboxymaltose Injection) is a sterile, preservative-free colloidal iron complex formulated for rapid intravenous iron replenishment. Each 10 mL vial contains 500 mg of elemental iron as ferric carboxymaltose, enabling high-dose iron administration in a single session.

Indications:
Foxifuse is indicated for the treatment of iron deficiency anemia (IDA) in adult and pediatric patients (14 years and older) who have:

• Intolerance to oral iron, or

• Unsatisfactory response to oral iron therapy, or

• Non-dialysis dependent chronic kidney disease (NDD-CKD).

Key Features:

• High-dose convenience: Up to 1,000 mg iron per infusion.

• Fast administration: Can be given over 15–30 minutes.

• Improved compliance: Fewer doses needed vs. traditional IV iron.

• Stable complex: Low risk of free iron release and oxidative stress.

 

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: Single Vial Per Box

Strength	10 IU/1 ML
Salt Type	LMWH
Packaging Type	Injection
Packaging Size	10 IU/ 1 ML
Manufacturer Name	SAMARTH LIFE SCIENCE PVT. LTD.
Brand Name	Caprin Flush
Product Name	Heparin Sodium Injection

Product Name: Heparin Sodium Injection
Brand Name: Caprin Flush
Strength: 10 IU/ 1 ML
Packing: Single Vial Per Box

Overview:

• Heparin Sodium Injection is an anticoagulant medication used to prevent blood clot formation.
• It is administered intravenously or subcutaneously to treat and prevent conditions such as deep vein thrombosis, pulmonary embolism, and myocardial infarction.

Mechanism of Action:

• Heparin works by enhancing the activity of antithrombin III, an endogenous anticoagulant, which inhibits the activity of thrombin and factor Xa, key components in the clotting cascade.

Indications:

• Prophylaxis and treatment of thromboembolic disorders.
• Prevention of clotting during certain medical procedures such as hemodialysis and extracorporeal circulation.
• Used in the management of acute coronary syndromes.

Dosage and Administration:

• Dosage varies based on the indication, patient weight, and coagulation status.
• Administered intravenously or subcutaneously.
• Dosage adjustments may be necessary in patients with renal impairment or other specific medical conditions.

Precautions and Side Effects:

• Risk of bleeding is the primary concern with heparin therapy.
• Close monitoring of coagulation parameters such as activated partial thromboplastin time (aPTT) or anti-Xa levels is necessary.
• Other potential side effects include heparin-induced thrombocytopenia, osteoporosis with long-term use, and hypersensitivity reactions.

Contraindications:

• Hypersensitivity to heparin or any component of the formulation.
• Active bleeding or high risk of bleeding.
• Severe thrombocytopenia.
• Intracranial hemorrhage.

Storage:

• Store at room temperature (15°C to 30°C or 59°F to 86°F).
• Protect from light.
• Do not freeze.
• Keep out of reach of children.

Additional Information:

• Packaging Details: SINGLE VIAL PER BOX

Strength	100 mg
Pack Size	5 ml Ampoule
Brand	FEROGEN
Packaging size	5 ml
Manufacturer	Samarth Life Sciences Pvt Ltd
Country of Origin	Made in India
Packing	5 Ampoules Per Box

Product Name: Iron Sucrose Injection USP
Brand Name: Roseiron
Strength: 100 MG/ 5ML
Packing: 5 Ampoules Per Box

Iron sucrose injection is a medication used to treat iron deficiency anemia, a condition where the body lacks enough iron to produce adequate red blood cells. Here's a brief description of iron sucrose injection:

1. Purpose: Treat iron deficiency anemia by replenishing iron stores in the body.

2. Administration: Administered via intravenous (IV) infusion by a healthcare professional in a clinical setting.

3. Mechanism of Action: Iron sucrose delivers iron directly into the bloodstream, where it is used by the body to produce hemoglobin and red blood cells.

4. Indications: Used when oral iron supplements are ineffective or cannot be tolerated, or when rapid iron replenishment is necessary.

5. Dosage: Dosage depends on the severity of the anemia and the patient's weight, usually administered in divided doses over several sessions.

6. Side Effects: Common side effects include headache, nausea, dizziness, and injection site reactions. Rarely, severe allergic reactions may occur.

7. Monitoring: Patients may require regular blood tests to monitor iron levels and response to treatment.

8. Contraindications: Iron sucrose may not be suitable for individuals with certain conditions such as iron overload disorders or hypersensitivity to the medication.

9. Precautions: Caution should be taken in patients with a history of allergies, asthma, or other allergic conditions.

10. Storage: Store iron sucrose injection at room temperature away from light and moisture.

11. Patient Education: Patients should be informed about the importance of completing the full course of treatment and any potential side effects to watch for.

12. Follow-Up: Patients may require follow-up appointments to assess treatment effectiveness and address any concerns or complications.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 5-6 weeks
• Packaging Details: 5 AMPOULES PER BOX

Strength	500000 I.U/Vial
Form	Solution
Brand	Dukinase
Packaging Type	Vial
Indication	Peripheral embolism, DVT, Catheter clearance, PE
Route of Administration	IV infusion
Usage	Hospital
Manufacturer	Samarth Life Science Pvt. Ltd
Usage / Application	Hospital
Shelf Life	24 to 36 Months
Storage Conditions	Recommended storage temperature: 2 DegreeC to 8 DegreeC (Refrigerated). Protect from light and avoid freezing.
Dose Strength	5000 IU

Product Name: Urokinase For Injection
Strength: 5000 IU
Brand Name: Dukinase
Packing: Single Vial Per Box

Indications:

Treatment of acute massive pulmonary embolism (PE)

Management of occluded intravenous or dialysis catheters

Acute myocardial infarction (AMI)

Deep vein thrombosis (DVT)

Peripheral arterial occlusion

Mechanism of Action:

Urokinase is a thrombolytic agent that converts plasminogen to plasmin, which breaks down fibrin clots.

It enhances fibrinolysis, promoting clot dissolution and improving blood flow.

Dosage and Administration:

Dosage varies based on the indication and patient’s condition.

Administered intravenously after reconstitution with sterile water or saline.

For catheter occlusion, the dose is typically smaller and directly instilled into the catheter.

Storage:

Store the lyophilized powder at room temperature, protected from light.

Once reconstituted, use immediately or store as per manufacturer’s instructions (typically, refrigerated and used within a few hours).

Additional Information:

• Production Capacity: 1000
• Delivery Time: 3-4 weeks
• Packaging Details: Single Vial Per Box

Concentration	99.9%
Strength	100 ML
Pack Volume	100 ml
Bottle Type	Clear Glass
Usage	muscle relaxation and reduces pains
Packaging Type	Vial
Grade	IP
Packaging Size	100ml
Brand	IFLURANE-100
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Prescription/Non-Prescription	Prescription

Product Name: Isoflurane Liquid for Inhalation
Brand Name: Iflurane-100
Strength: 100 ML
Packing: Single Bottle Per Box

Product Description:

Iflurane-100 is a potent, non-flammable, halogenated ether-based general anesthetic used for the induction and maintenance of general anesthesia. It is widely used in both adult and pediatric surgical procedures due to its predictable pharmacokinetics, rapid onset, and ease of depth adjustment during anesthesia. Isoflurane is known for maintaining cardiovascular stability and providing excellent muscle relaxation.

Composition:

• Each 100 mL contains:

  • Isoflurane USP – 100 mL

• Appearance: Clear, colorless, volatile liquid with a mild ethereal odor

Mechanism of Action:

Isoflurane acts primarily by enhancing GABA-A receptor activity, leading to suppression of neuronal excitability and central nervous system depression. It decreases the rate of depolarization of action potentials, resulting in unconsciousness and muscle relaxation. Isoflurane also depresses pain perception and memory during surgical procedures.

Indications:

• Induction of general anesthesia

• Maintenance of general anesthesia during surgical operations

• Suitable for use in adult and pediatric patients

Key Benefits:

• Rapid onset and smooth induction

• Allows quick adjustment of anesthesia depth

• Minimal metabolism (<0.2%), reducing hepatic burden

• Maintains cardiac output with minimal myocardial depression

• Provides muscle relaxation, reducing need for additional agents

Dosage & Administration:

• Administer via a precision-calibrated vaporizer designed for isoflurane delivery.

• Induction: Typically 1.5%–3.0% concentration in oxygen or oxygen/nitrous oxide mix

• Maintenance: Generally 1.0%–2.5%, titrated to desired anesthetic depth

•  

Additional Information:

• Production Capacity: 100
• Packaging Details: SINGLE BOTTLE PER BOX

Strength	2 mg/ml
Pack Type	Ampoule
Brand Name	ISOLIN
Packaging Type	Box
Form	Injection
Manufacturer	SAMARTH LIFE SCIENCE PVT. LTD.
Country of Origin	Made in India

Product Name: Isoprenaline HCL Injection IP
Brand Name: Isolin
Strength: 2 MG/ 1 ML
Packing:5 Ampoules Per Box

Isoprenaline HCL Injection IP is a medication primarily used in emergency situations to address certain cardiac conditions and respiratory distress. Here's a concise overview of its key features:

• Medical Use: Isoprenaline HCL Injection IP is administered to manage severe cases of bradycardia (slow heart rate), heart block, and bronchospasm (narrowing of the airways).

• Mechanism of Action: It works by stimulating beta-adrenergic receptors, leading to increased heart rate (positive chronotropic effect), improved cardiac output, and bronchodilation.

• Emergency Situations: This medication is particularly valuable in emergency settings such as cardiac arrest, where rapid intervention is crucial to restore normal heart rhythm and function.

• Dosage Form: Isoprenaline HCL Injection IP is provided in a sterile solution form for intravenous administration, ensuring fast and reliable absorption into the bloodstream.

• Medical Supervision: Administration of this medication should be performed under the supervision of healthcare professionals due to its potent effects on cardiac and respiratory systems.

• Side Effects: Common side effects may include palpitations, tremors, headache, and increased blood pressure. Serious adverse reactions such as arrhythmias may occur, necessitating close monitoring during administration.

• Contraindications: Isoprenaline HCL Injection IP is contraindicated in patients with known hypersensitivity to the drug, as well as in those with certain cardiac conditions such as ventricular tachycardia and untreated heart failure.

• Storage: It should be stored in a cool, dry place away from direct sunlight and out of reach of children, following manufacturer's instructions to maintain its efficacy and safety.

Isoprenaline HCL Injection IP serves as a vital tool in emergency medical care, providing rapid and targeted intervention in critical situations affecting cardiac and respiratory function.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 WEEKS
• Packaging Details: 5 AMPOULES PER BOX

Strength	200 mg
Brand	Samarth Life Scinces Pvt Ltd
Treatment	Cardiac Arrhythmias
Dose/Strength	200mg
Manufacturer	Samarth Life Science Pvt Ltd
Packaging Size	10 x 10 tablets
Shelf Life	24 months
Grade Standard	Medicine Grade
Generic Name	AMIODERONE TABLETS BP

Product Name: Amiodarone Tablets IP
Brand Name: Duron 
Strength: 200 MG
Packing: 100 Tablets Per Box

Amiodarone Tablets are a medication primarily used to treat certain types of irregular heartbeats, known as arrhythmias. This medication belongs to the class of drugs called antiarrhythmics, which work by stabilizing the heart's electrical activity. Amiodarone Tablets are commonly prescribed for serious arrhythmias such as ventricular fibrillation and ventricular tachycardia. They help restore normal heart rhythm and reduce the risk of life-threatening complications. However, due to potential side effects and interactions with other medications, Amiodarone Tablets should be used under the supervision of a healthcare professional.

Description:Amiodarone, an antiarrhythmics produces its helpful effects by slowing heart nerve impulses and acting directly on the heart tissues.

Indications: Amiodarone is an effective agent for the management of supraventricular and ventricular arrhythmias. It is indicated in controlling both atrial and ventricular arrhythmias associated with hypertrophic cardiomyopathy and may reduce the incidence of sudden death in these patients. DURON has been reported to improve mortality rates in patients surviving myocardial infarction.

Storage: Store at a temperature below 25°C. Protect from light and moisture.

Presentation: A box containing 6 blisters of 10 tablets each of Amiodarone HCl 200 mg.

Form	Capsule
Release Type	Prolonged Release
Brand	Pro Hype SR
Strength	20 mg
Pack Size	10*10 Tablet
Treatment	Hypertension
Brand Name	Pro Hype SR
Manufacturer	Samarth Life Science Pvt. Ltd
Country of Origin	Made in India
Pack Type	Box
Packaging Type	Strip

Product Name: Propranolol Prolonged relase Capsules IP
Brand Name: Pro Hype SR
Strength:20 MG
Packing:100 Capsules Per Box

Product Description:

 

ProHype SR 20 mg contains Propranolol Hydrochloride, a non-selective beta-adrenergic blocker formulated in a sustained-release capsule for once-daily dosing. It works by reducing the heart rate, myocardial contractility, and blood pressure, providing effective management of several cardiovascular and neurologic conditions.

Mechanism of Action:Propranolol is a non-selective beta-blocker that blocks both β1 and β2 adrenergic receptors. It decreases sympathetic nervous system stimulation of the heart, reducing heart rate, cardiac output, and renin release. The prolonged-release formulation ensures controlled plasma levels over 24 hours, improving adherence and therapeutic outcomes.Storage:Store below 25°C. Protect from light and moisture.Keep out of reach of children.

 

Additional Information:

• Item Code: POLY-B
• Delivery Time: 4-5 WEEKS
• Packaging Details: 100 Capsules Per Box

Strength	20 mg/ 4 ml
Vial Volume	4 ml
With Dextrose	With Dextrose
Packaging Size	4ml
Route	Spinal
Pack Type	Ampoule
Packaging type	Ampoule
Brand	NUMBCAINE HEAVY
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Prescription/Non-Prescription	Prescription
Country of Origin	Made in India

Product Name: Bupivacaine Hydrochloride in Dextrose Injection
Brand Name: Numbcaine Heavy
Strength: 20 MG/ 4 ML
Packing: 5 Ampoules Per Box

Product Description:
NUMBCAINE HEAVY by Genex Pharma is a sterile, hyperbaric spinal anesthetic solution containing Bupivacaine Hydrochloride 0.5% (20 mg/4 mL) with 8% Dextrose. It is specially formulated for safe and effective intrathecal anesthesia in surgical, obstetric, and gynecological procedures.

Indications:

• Regional anesthesia for lower abdominal, pelvic, and lower limb surgeries

• Obstetric procedures including Cesarean section

• Urological and gynecological interventions

Benefits of NUMBCAINE HEAVY (by Genex Pharma):

• Rapid onset with long-lasting spinal block

• Hyperbaric formulation ensures predictable spread

• Reliable sensory and motor block

• Backed by Genex Pharma’s commitment to safety and quality

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: 5 Ampoules Per Box

Concentration	99.9%
Strength	250 mg
Pack Volume	250 ml
Bottle Type	Clear Glass
Usage	Inhalation
Packaging Type	Bottle
Grade	IP
Packaging Size	250ml
Brand	IFLURANE-250
Country of Origin	Made in India
Brand Name	Iflurane 250

Product Name: Isoflurane Liquid For Inhalation IP
Brand Name: Iflurane 250 
Strength: 250 ML
Packing:Single Bottle Per Box

• Isoflurane Liquid For Inhalation IP 250 ML is a potent inhalation anesthetic utilized for inducing and maintaining general anesthesia during surgical procedures.
• This formulation is intended for inhalation administration through specialized vaporizers, facilitating precise control over anesthesia depth.
• Isoflurane is classified as a halogenated ether, exerting its anesthetic effect by depressing the central nervous system.
• The 250 milliliter container holds the liquid form of isoflurane, which is vaporized into a gas before being inhaled by the patient.
• Its rapid onset and offset of action make isoflurane a preferred choice for anesthesia management, allowing for swift adjustment during procedures.
• Proper dosage and administration are imperative and should be overseen by trained anesthesia professionals to ensure patient safety and optimal anesthesia depth.
• Side effects may include respiratory depression, hypotension, and postoperative nausea and vomiting.
• Due to its flammable nature, isoflurane should be stored and handled with caution, away from heat sources.

Additional Information:

• Packaging Details: SINGLE BOTTLE PER BOX

Strength	200 mg
Brand	Samarth Life Scinces Pvt Ltd
Packaging Size	5 ml
Pack Type	Ampoule
Shelf Life	24 months
Dose/Strength	200mg / 5ml
Packaging Type	Ampoule
Pharmacopoeia Standard	IP
Generic Name	DOPAMINE HYDROCHLORIDE INJECTION
Country of Origin	Made in India

Product Name: Dopamine HCL Injection
Brand Name: Dopar
strength: 200 mg/ 2ml
Packing: 25 Ampoules Per Box

• Drug Class: Dopaminergic Agent, Inotropic Agent
• Purpose: Used to increase blood pressure and cardiac output in conditions such as shock, heart failure, and low blood pressure due to various causes.
• Administration: Administered intravenously.
• Mechanism of Action:
  • Stimulates dopamine receptors in the body, leading to increased heart rate and contractility, vasodilation in renal and splanchnic circulations, and vasoconstriction in peripheral blood vessels.
  • Different dosages produce different effects: low doses primarily affect renal and splanchnic vasodilation, intermediate doses increase cardiac output, and high doses result in vasoconstriction.
• Indications:
  • Used in the management of shock (e.g., septic shock, cardiogenic shock).
  • Employed as a vasopressor in patients with hypotension.
• Dosage:
  • Dosage varies based on the indication, patient's hemodynamic status, and individual response to treatment.
  • Typically administered as a continuous infusion.
• Precautions:
  • Monitor closely for extravasation as it can cause tissue necrosis.
  • Use with caution in patients with arrhythmias, hypertension, or peripheral vascular disease.
• Contraindications:
  • Hypersensitivity to dopamine or any components of the formulation.
  • Pheochromocytoma (a rare tumor of adrenal gland tissue).
• Adverse Effects:
  • Common adverse effects include tachycardia, arrhythmias, hypertension, headache, and nausea.
  • Extravasation can lead to tissue necrosis.
• Special Populations:
  • Use with caution in elderly patients and those with pre-existing cardiovascular conditions.
  • May exacerbate underlying arrhythmias or ischemic heart disease.
• Storage:
  • Store at controlled room temperature.
  • Protect from light.
• Drug Interactions:
  • Concurrent use with monoamine oxidase inhibitors (MAOIs) or tricyclic antidepressants may increase the risk of hypertensive crisis.
  • Beta-blockers may attenuate the effects of dopamine.
• Monitoring:
  • Continuous monitoring of blood pressure, heart rate, and ECG during administration.
  • Regular assessment of urine output and renal function.
• Patient Counseling:
  • Inform patients about the purpose of the medication and potential side effects.
  • Instruct patients to report any adverse reactions or changes in symptoms promptly.

Additional Information:

• Packaging Details: 25 AMPOULES PER BOX

Strength	100 mg
Dose/Strength	100 mg
Pack Size	50 Tablets
Pharmacopeia Standard	BP
Packaging Size	50 Tablets
Brand	Lobet
Usage / Application	Hospital
Shelf Life	24 Months
Packaging Type	Strip

Product Name: Lobetalol Tablet
Brand Name: Lobet
Strength: 100 MG
Packing: 50 Tablets Per Box

_{Product Description}

Lobet (Labetalol Tablets 100 mg) by Genex Pharma is an oral antihypertensive medication belonging to the class of combined alpha- and beta-adrenergic receptor blockers. Labetalol effectively lowers blood pressure by reducing systemic vascular resistance (alpha-blockade) and decreasing heart rate and cardiac output (beta-blockade). Unlike conventional beta-blockers, it provides balanced blood pressure control with minimal effect on resting heart rate and cardiac output, making it a reliable option for both acute and long-term management of hypertension.

Indications

Lobet 100 mg is indicated for:

• Hypertension (Primary/Essential and Secondary): Long-term management of mild to severe high blood pressure

• Hypertensive emergencies (oral step-down after IV therapy)

• Pregnancy-induced hypertension (PIH) / Preeclampsia (where appropriate, under specialist supervision)

• Angina pectoris and other conditions where reduction of myocardial oxygen demand is beneficial

_Storage

• Store below 25°C in a dry place

• Protect from light and moisture

• Keep out of reach of children

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 Weeks
• Packaging Details: 50 Tablets Per Box

Strength	100 mcg
Brand	Dexmedine
Packaging Size	1 ml
Packaging Type	Ampoule
Usage/Application	ICU Sedation
Form	Injection
Prescription/Non prescription	Prescription
Composition	Dexmedetomidine

Product Name: Dexmedetomidine Hydrochloride Injection
Brand Name:vDexmedine
Strength: 100 MCG/1ML
Packing:A Single Ampoules Per Box

Product Overview
DEXMEDINE (Dexmedetomidine Hydrochloride Injection) is a highly selective α2-adrenergic receptor agonist used for sedation in intensive care and procedural settings. It provides controlled sedation with minimal respiratory depression, making it an ideal choice for critically ill patients requiring continuous monitoring and comfort.

Composition
Each 1 mL ampoule contains:

• Dexmedetomidine Hydrochloride equivalent to Dexmedetomidine 100 mcg

• Sterile aqueous solution for intravenous administration

Additional Information:

• Production Capacity: 10000
• Delivery Time: 5-6 Weeks
• Packaging Details: A Single Ampoule Per Box

Strength	250mg/5ml
Pack Size	5 ml
Brand	Samarth
Composition	Dobutamine HCl
Form	Injection
Packaging Type	Ampoule
Brand Name	Dobustat
Manufactured By	Samarth Science Pvt. Ltd
Country of Origin	Made in India

Product Name: Dobutamine HCL Injection
Brand Name: Dobustat
Strength: 250mg/5ml
Packing:2 Ampoules Per Box

Product Description:

DOBUSTAT (Dobutamine Hydrochloride Injection 250 mg/5 mL) is a fast-acting, sterile intravenous inotropic agent used to manage acute heart failure, cardiogenic shock, and low cardiac output states following cardiac surgery or myocardial infarction. Manufactured by Genex Pharma, DOBUSTAT is formulated to improve heart muscle contractility and increase cardiac output with minimal effect on heart rate and blood pressure.

Each 5 mL ampoule contains 250 mg of Dobutamine HCl (50 mg/mL) and is intended to be diluted before IV infusion. It is widely used in emergency departments, ICUs, and cardiac care units.

Key Features:High-concentration formulation: 250 mg/5 mL (50 mg/mL)Rapid onset and short duration of actionEnhances cardiac output without significant vasoconstrictionManufactured under WHO-GMP certified facilitySuitable for emergency and critical care settingsIndications:Acute congestive heart failureCardiogenic shockLow output syndrome post-cardiac surgerySupportive therapy in cardiac decompensationStorage Instructions:Store below 25°CProtect from direct sunlightDo not freezeUse immediately after dilution

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: 2 AMPOULES PER BOX

Strength	100 mg
Pack Size	5 ml Ampoule
Brand	Roseiron
Packaging size	5 ml
Usage	To treat iron deficiency anemia
Manufacturer	Samarth Life Science Pvt. Ltd
Prescription/Non Prescription	Prescription
Also gives	Pharmaceutical Third Party Manufacturing
Shelf life	36 Months
Country of Origin	Made in India

Product Name: Iron Sucrose Injection
Brand Name: Roseiron
Strength: 100 MG/ 5 ML
Packing: 5 Ampoules Per Box

_{Product Description:}

ROSEIRON (Iron Sucrose Injection 100 mg/5 mL) by Genex Pharma is a parenteral iron preparation used for the treatment of iron deficiency anemia (IDA) in patients who are intolerant to or have had an unsatisfactory response to oral iron therapy. It replenishes depleted iron stores efficiently and supports red blood cell production, particularly in patients with chronic kidney disease (CKD), pregnancy, or those undergoing hemodialysis.

_Indications:

ROSEIRON is indicated for:

• Iron deficiency anemia in adults and pediatric patients aged 2 years and above

• Anemia associated with chronic kidney disease (CKD)

• Anemia during pregnancy, especially in cases of poor tolerance or response to oral iron

• Postpartum iron deficiency

• Iron deficiency in patients undergoing hemodialysis or peritoneal dialysis

_{Mechanism of Action:}

Iron Sucrose is composed of a polynuclear iron(III)-hydroxide complex stabilized with sucrose. After intravenous administration, it is absorbed by the reticuloendothelial system and then incorporated into hemoglobin in the bone marrow, thus helping to restore normal red blood cell production.

_{Product Highlights:}

✅ Effective for rapid replenishment of iron stores
✅ Safe for CKD and dialysis patients
✅ No test dose required
✅ Manufactured under strict WHO-GMP guidelines
✅ Available for domestic and export markets

 

Additional Information:

• Production Capacity: 1000
• Delivery Time: 5-6 weeks
• Packaging Details: 5 AMPOULES PER BOX

Strength	5 G/20 ML
Composition	Somatropin (HGH)
Pack Size	20ML
Pack Type	Vial
Route	IV
Packaging Size	1 Vial
Grade	IP
Dosage Form	Pre-filled Syringe
Sugar Free	Yes
Brand Name	HAMOSTAT
Manufacturer	Samarth Life Science Pvt. Ltd
Injection Routes	Subcutaneous (SC)
Country of Origin	Made in India
Packing	Single Vial Per Box

Product Name: Aminocaproic Acid Injection IP
Brand Name: Hamostat
Strength: 5 GM/ 20 ML
Packing: Single Vial Per Box

Aminocaproic Acid Injection IP is a medication primarily used to control bleeding in various clinical settings. Here's a concise overview with pointers:
Medical Use: Administered to manage or prevent excessive bleeding in conditions such as surgical procedures, trauma, and certain medical conditions like hemophilia.

Mechanism of Action: Functions as an antifibrinolytic agent by inhibiting the activation of plasminogen, thus preventing the breakdown of fibrin clots and reducing bleeding.Dosage Form: Provided as a sterile solution for intravenous administration, ensuring rapid delivery and onset of action.

Onset of Action: Rapid onset of action allows for quick control of bleeding, making it valuable in emergency situations.
Medical Supervision: Administration should be under the supervision of healthcare professionals experienced in hemostasis management, as dosing and monitoring are crucial to prevent complications such as thrombosis or allergic reactions.

Side Effects: Common side effects may include nausea, vomiting, and diarrhea. Rare but serious adverse reactions such as thromboembolism may occur.Contraindications: Avoid in patients with a history of thromboembolic events, renal impairment, or hypersensitivity to aminocaproic acid.

Storage: Store in a cool, dry place, away from sunlight and out of reach of children, following manufacturer's instructions to maintain efficacy and safety.Aminocaproic Acid Injection IP is an essential medication in the management of bleeding disorders, providing rapid control of hemorrhage while minimizing systemic side effects.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE VIAL PER BOX

Packaging Type	Vial
Strength	150 mg
Concentration Type	Concentrate
Route of Administration	Intravenous
Brand	DURON
Packaging Size	3 ml
Dose/Strength	150 mg
Manufacturer	Samarth Life Science Pvt. Ltd.

Product Name: Amiodarone HCI Injection
Brand Name: Duron
Strength: 150 MG/ 3 ML
Packing: 5 Ampoules

DESCRIPTION: Amiodarone is a class III antiarrhythmic drug.
INDICATIONS: Amiodarone is indicated for initiation of treatment and prophylaxis of frequently recurring ventricular fibrillation and hemodynamically unstable ventricular tachycardia in patients refractory to other therapy. Amiodarone also can be used to treat patients with VT/VF who are unable to take oral medication. Amiodarone should also be used for acute treatment until the patient's ventricular arrhythmias are stabilized.
STORAGE: Store at a temperature not exceeding 25°C. Protect from light.
PRESENTATION: A box containing 5 ampuoles of 3ml each.
Purpose: Used for the treatment of life-threatening recurrent ventricular fibrillation or hemodynamically unstable ventricular tachycardia when oral therapy is not feasible.
Dosage Strength:Available typically in a concentration of 50 mg/mL.
Mechanism of Action:Works by blocking certain electrical signals in the heart, helping to restore normal heart rhythm.
Administration:Administered intravenously by a healthcare professional in a hospital or clinical setting.
Indications:Used for the acute treatment of ventricular arrhythmias when prompt control of arrhythmia is required.
Contraindications:Patients with severe sinus node dysfunction, second- or third-degree atrioventricular block, and known hypersensitivity to amiodarone or iodine.
Side Effects:Common side effects may include hypotension, bradycardia, nausea, vomiting, and dizziness.
Serious Side Effects:Rare but serious side effects may include pulmonary toxicity, liver toxicity, thyroid dysfunction, and vision problems.
Precautions:Regular monitoring of vital signs, heart rhythm, electrolyte levels, lung function, liver function, and thyroid function is essential during treatment.

Additional Information:

• Packaging Details: 5 AMPOULES PER BOX

Composition	Digoxin
Strength	0.5mg/2ml
Dose	0.5 mg
Pharmacopoeia Standard	IP
Brand	DIXIN
Pack Size	2 ml
Pack Type	Box
Manufacturer	Samarth Life Science Pvt. Ltd
Packaging Type	Ampoule
Brand Name	DIXIN

Product Name: Digoxin Injection
Brand Name: Dixin
Strength: 0.5 MG/ 2 ML
Packing: 10 Ampoules Per Box

Digoxin Injection belongs to the class of cardiac glycosides.It reduces strain on the heart and helpsit maintain a normal,steady, and strong heatbeat.


Main Use: Primarily prescribed for managing heart failure, atrial fibrillation, and certain heart rhythm irregularities.

Mode of Action: Operates by enhancing the force of heart muscle contractions and moderating heart rate.

Administration: Typically administered through intravenous (IV) injection.

Usage Situations: Employed in acute scenarios for swift heart rate regulation or when oral ingestion is impractical.

Speed of Effect: Its impact is promptly observed, usually within 5-30 minutes.

Duration of Effect: Lasts for several hours to days, contingent on individual patient characteristics.

Monitoring Requirement: Regular monitoring of blood levels is essential to ensure therapeutic effectiveness and prevent toxicity.

Side Effects: Common side effects encompass nausea, vomiting, headache, and potential visual disturbances; excessive levels may induce severe cardiac arrhythmias.

Contraindications: Contraindicated in cases of digoxin hypersensitivity, ventricular fibrillation, and specific heart block conditions.

Special Considerations: Dosage adjustments might be warranted for patients with kidney dysfunction or electrolyte imbalances.

Drug Interactions: Potential interactions with medications influencing heart rhythm or electrolyte levels, such as diuretics or other cardiac drugs.

Patient Guidance: Emphasize the importance of adhering to prescribed dosages, recognizing signs of toxicity (like nausea, vomiting, or visual disturbances), and scheduling regular follow-ups with healthcare providers for monitoring purposes.

Storage: Store at a temperature below 25 C. Protect from light and moisture.

Presentation:
Digoxin Injecion 0.5 ml/2ml
Each pack contains 10 ampoulesof 2ml each.

Additional Information:

• Packaging Details: 10 AMPOULES PER BOX

Indication	Cough Cold
Composition	Multivitamin
Strength	3mg /60ml
Brand	DIXIN PAED
Packaging Size	Single Bottle Per Box
Packaging Type	Bottle
Age Group	Paediatric
Flavour	Mixed Fruit
Usage/Application	Commercial
Dose	60 ML
Generic Name	Digoxin Paediatric Solution
Country of Origin	Made in India

Product Name: Digoxin Pediatric Syrup
Brand Name: Dixin
Strength: 3 MG/ 60 ML
Packing: Single Bottle Per Box

Digoxin pediatric solution IP is a medication primarily used to treat heart conditions in children, such as congestive heart failure and certain arrhythmias. Here's a concise description with pointers:

Purpose: Treats heart conditions in pediatric patients, including congestive heart failure and certain arrhythmias.

Administration: Administered orally as a solution, usually in a hospital or clinical setting.

Mechanism of Action: Digoxin increases the force of heart muscle contractions and slows down the heart rate, improving heart function.

Indications: Used in pediatric patients with heart failure, atrial fibrillation, and supraventricular tachycardia.

Dosage: Dosage is based on the child's weight, age, and medical condition, administered in divided doses.

Onset and Duration: Onset of action is usually within 30 minutes to 2 hours, with effects lasting for about 24 hours.

Side Effects: Common side effects may include nausea, vomiting, loss of appetite, and arrhythmias. Risk of toxicity exists, especially in infants and young children.

Contraindications: Avoid use in patients with ventricular fibrillation, severe heart block, or hypersensitivity to digoxin.

Precautions: Care should be taken in pediatric patients with impaired kidney function or electrolyte imbalances.

Storage: Store digoxin pediatric solution according to manufacturer instructions, typically at controlled room temperature and protected from light.

Patient Monitoring: Regular monitoring of heart rate, electrolytes, and digoxin levels is necessary to ensure therapeutic efficacy and prevent toxicity.

Education: Caregivers should be educated on proper administration techniques, signs of toxicity, and the importance of adherence to the prescribed dosage regimen.

Additional Information:

• Production Capacity: 12000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE BOTTLE PER BOX

Dosage Form	Syrup
Indication	Hepatic
Packaging Size	30 ml
Composition Type	Combination
Age Group	Paediatric Adult
Flavour	Pineapple
Usage/Application	Clinical
Dose/Strength	300 MG / 30 ML
Country of Origin	Made in India
Brand Name	Furoped
Packing	Single Bottle Per Box

Product Name: Furosemide Oral Solution USP
Brand Name: Furoped
Stregth: 300 MG/ 30 ML
Packing: Single Bottle Per Box

Furosemide Oral Solution Overview:

• Purpose: Used to treat edema associated with congestive heart failure, liver cirrhosis, and renal disease, as well as hypertension.
• Formulation: Available as a liquid oral solution.
• Administration: Administered orally.
• Mechanism of Action:
  • Inhibits the reabsorption of sodium and chloride in the ascending loop of Henle in the kidneys, leading to increased excretion of water, sodium, chloride, and other electrolytes.
• Indications:
  • Treatment of edema associated with heart failure, liver cirrhosis, renal disease, and other conditions.
  • Management of hypertension.
• Dosage:
  • Dosage varies depending on the individual patient's condition, weight, and response to treatment.
  • Typically administered once or twice daily.
• Precautions:
  • Monitor electrolyte levels (especially potassium), renal function, and blood pressure regularly during treatment.
  • Use caution in patients with severe electrolyte disturbances, dehydration, or hepatic impairment.
• Contraindications:
  • Hypersensitivity to furosemide or any components of the formulation.
  • Anuria (lack of urine production).
• Adverse Effects:
  • Common adverse effects include electrolyte imbalances (hypokalemia, hyponatremia), dehydration, hypotension, and ototoxicity.
  • Rare but serious adverse effects may include renal dysfunction, thrombocytopenia, and Stevens-Johnson syndrome.
• Special Populations:
  • Use with caution in elderly patients and those with impaired renal function or electrolyte abnormalities.
  • Pregnancy category C – weigh benefits against risks before use during pregnancy.
• Storage:
  • Store at controlled room temperature away from moisture and heat.
  • Protect from light.
• Drug Interactions:
  • Concurrent use with other medications that affect electrolyte balance or renal function may increase the risk of adverse effects.
  • May potentiate the effects of other antihypertensive drugs.
• Monitoring:
  • Regular monitoring of electrolytes, renal function, and blood pressure.
  • Periodic assessments of fluid status and weight.
• Patient Counseling:
  • Take the medication exactly as prescribed by the healthcare provider.
  • Avoid sudden changes in fluid intake to prevent dehydration.
  • Report any signs of electrolyte imbalance (muscle weakness, irregular heartbeat) or adverse reactions promptly.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE BOTTLE PER BOX

Strength	100mg/10ml
Brand	ESOCARD
Packaging Size	10ml
Treatment	Hypertension
Manufacturer	Samarth Life Science Pvt Ltd
Form	Injection
Packaging Type	Vial
Generic	Esmolol Injection
Manufactured By	Samarth Life Sciences Pvt Ltd.

Product Name: Esmolol Hydrochloride Injection 100 MG
Brand Name: Esocard
Strength: 100 MG/ 10 MLDescription:

ESOCARD (Esmolol Hydrochloride Injection) is a short-acting, cardioselective beta-1 adrenergic receptor blocker, formulated for intravenous administration. It is primarily used in clinical settings where rapid onset and short duration of beta-blockade are desired, such as acute arrhythmias and perioperative tachycardia or hypertension.

Composition:

Each mL contains:

• Esmolol Hydrochloride USP equivalent to 10 mg Esmolol

• Water for Injection IP q.s.

Available strengths:

• 10 mg/mL in 10 mL ampoule or vial

Indications:

ESOCARD is indicated for:

• Supraventricular tachycardia (SVT)

• Non-compensatory sinus tachycardia

• Intraoperative and postoperative tachycardia and/or hypertension

• Atrial fibrillation or atrial flutter with rapid ventricular response

Mechanism of Action:

Esmolol is a beta-1 selective (cardioselective) adrenergic receptor blocker that rapidly reduces heart rate and myocardial contractility by inhibiting the response to adrenergic stimulation. Its short half-life (approx. 9 minutes) allows precise titration and quick reversal upon discontinuation.

Packing: Single Vial Per Box


 

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE VIAL PER BOX

Route of Administration	Intravenous
Brand	LOBET
Form	Injection
Manufacturer	Samarth Life Science Pvt. Ltd.
Country of Origin	Made in India
Packaging Size	4 ml
Strength	20 mg

Product Name: Labetalol HCL Injection
Brand Name: Lobet
Strength: 100 MG /20 ML
Packing: 2 Ampoules Per Box

Labetalol Injection IP 100 MG/20 ML is a medication primarily used to manage hypertension and hypertensive emergencies. Here's a concise overview of its key features:

• Medical Use: Labetalol Injection IP 100 MG/20 ML is administered to lower blood pressure in hypertensive emergencies, including severe hypertension during pregnancy (pre-eclampsia and eclampsia).

• Dual Action: Combines both selective beta-blocking and alpha-blocking properties, leading to vasodilation and reduced heart rate, effectively lowering blood pressure.

• Dosage Strength: Each 20 mL ampoule contains 100 mg of Labetalol, providing a standardized dose for intravenous administration.

• Onset of Action: Typically begins to lower blood pressure within minutes of administration, making it suitable for acute management of hypertensive crises.

• Medical Supervision: Administration should be under close supervision of healthcare professionals in a monitored setting due to potential significant changes in blood pressure and heart rate.

• Side Effects: Common side effects may include dizziness, fatigue, and bradycardia. Hypotension and bronchospasm may occur, especially in patients with asthma or COPD.

• Contraindications: Avoid in severe bradycardia, heart block greater than first degree, cardiogenic shock, or decompensated heart failure.

• Storage: Store in a cool, dry place, away from sunlight and out of reach of children, following manufacturer's instructions to maintain efficacy and safety.

Labetalol Injection IP 100 MG/20 ML is an essential tool in the acute management of hypertensive emergencies, providing rapid and effective blood pressure control in critical situations.

Additional Information:

• Packaging Details: SINGLE AMPOULE PER BOX

Packaging Size	4 ml
Route of Administration	Intravenous
Brand	LOBET
Strength	20 mg
Packaging Type	Box
Form	Injection

Product Name: Labetalol Injection IP 20 MG
Brand Name: Lobet
Strength: 20 MG/ 4 ML
Packing: 2 Ampoules Per Box

Labetalol Injection IP 20 MG is a medication primarily used to manage hypertension and hypertensive emergencies. Here's a concise overview of its key features:

• Medical Use: Labetalol Injection IP 20 MG is administered to lower blood pressure in hypertensive emergencies, including severe hypertension during pregnancy (pre-eclampsia and eclampsia).

• Dual Action: It combines both selective beta-blocking and alpha-blocking properties, leading to vasodilation and reduced heart rate, thus effectively lowering blood pressure.

• Dosage Form: Labetalol Injection IP 20 MG is provided in a sterile solution form for intravenous administration, ensuring rapid onset of action in emergency situations.

• Onset of Action: It typically begins to lower blood pressure within minutes of administration, making it suitable for acute management of hypertensive crises.

• Medical Supervision: Administration of this medication should be performed under the close supervision of healthcare professionals in a monitored setting due to its potential to cause significant changes in blood pressure and heart rate.

• Side Effects: Common side effects may include dizziness, fatigue, and bradycardia. Hypotension (low blood pressure) and bronchospasm may occur, particularly in patients with asthma or chronic obstructive pulmonary disease (COPD).

• Contraindications: Labetalol Injection IP 20 MG is contraindicated in patients with severe bradycardia, heart block greater than first degree, cardiogenic shock, or decompensated heart failure.

• Storage: It should be stored in a cool, dry place away from direct sunlight and out of reach of children, following manufacturer's instructions to maintain its efficacy and safety.

Labetalol Injection IP 20 MG plays a crucial role in the acute management of hypertensive emergencies, providing rapid and effective blood pressure control in critical situations.

Additional Information:

• Packaging Details: 2 AMPOULES PER BOX

Strength	1g/5ml
Pack Size	5 ml
Brand	Vocartine
Form	Drops
Pack Type	Ampoule
Brand Name	Vocartine
Manufacturer	SAMARTH LIFE SCIENCE PVT. LTD

Product Name: Levocarnitine Injection USP
Brand Name: Vocartine
Strength: 1G/5 ML
Packing: 5 Ampoules Per Box

Levocarnitine Injection is a medication primarily used to treat carnitine deficiency and certain metabolic disorders. Here's a concise overview with pointers:

• Medical Use: Administered to correct deficiencies in carnitine, a substance necessary for the metabolism of fatty acids.

• Mechanism of Action: Works by replenishing carnitine levels in the body, facilitating the transport of fatty acids into the mitochondria for energy production.

• Dosage Form: Provided as a sterile solution for intravenous or intramuscular administration, ensuring rapid delivery and absorption.

• Indications: Used in conditions such as primary systemic carnitine deficiency, secondary carnitine deficiency due to certain medications or metabolic disorders, and dialysis-associated carnitine deficiency.

• Medical Supervision: Administration should be under the guidance of healthcare professionals experienced in the management of metabolic disorders, as dosing and monitoring are essential to prevent complications.

• Side Effects: Common side effects may include nausea, vomiting, and diarrhea. Rare but serious adverse reactions such as allergic reactions or seizures may occur.

• Contraindications: Avoid in patients with known hypersensitivity to levocarnitine or other ingredients in the formulation.

• Storage: Store in a cool, dry place, away from sunlight and out of reach of children, following manufacturer's instructions to maintain efficacy and safety.

Levocarnitine Injection plays a crucial role in correcting carnitine deficiencies, aiding in the management of metabolic disorders and supporting energy metabolism.

Additional Information:

• Packaging Details: 5 AMPOULES PER BOX