Genex Pharma

Strength	50mg/5ml
Vial Volume	5 ml
Pack Type	Ampoule
Route	IV
Pack Size	Single Vial
Brand	ATRAPURE
Packaging Type	Ampoule
Manufacturer	Samarth Life Sciences Pvt Ltd
Injection Administeration Type	IV only
Country of Origin	Made in India

Product Name:Atracurium Besylate Injection
Brand Name:Atrapure
Strength: 50 mg/5 ml
Packing: 5 Ampoule Per Box

Product Description:
Atrapure is a non-depolarizing neuromuscular blocking agent used to achieve skeletal muscle relaxation during surgical procedures or mechanical ventilation. It is commonly used as an adjunct to general anesthesia to facilitate endotracheal intubation and optimize surgical conditions.
Indications:

Atrapure is indicated for:

• Use as an adjunct to general anesthesia to facilitate endotracheal intubation

• Providing skeletal muscle relaxation during surgery

• Muscle relaxation in patients requiring mechanical ventilation in intensive care units

Storage Instructions:

• Store between 2°C and 8°C

• Do not freeze

• Protect from light

Presentations Available:

Atrapure (Atracurium Besylate Injection) is available in multiple strengths and packaging options:

• 25 mg/2.5 mL – Pack of 5 ampoules

• 50 mg/5 mL – Pack of 5 ampoules

• 100 mg/10 mL – Single vial per box

 

Packaging Size	5 ml
Strength	10 mg/ml
Concentration	10mg/5ml
Prescription/Non prescription	Prescription
Packaging Type	Vial
Brand	Samarth Life Science Pvt. Ltd.
Shelf Life	18 months
Also gives	PCD Pharma
Usage	Used as general anesthesia
Country of origin	Made in India

Product Name:Cisatracurium Besylate Injection
Brand Name: Atracis
Strength: 10 MG/ 5 ML
Packing: Single Vial Per Box

Cisatracurium Besylate is a nondepolarizing skeletal neuromuscular blocking agent (NMBA) and is intermediate in its onset & duration of action.

Indication: Used for skeletal muscle relaxation during surgery in children aged 1 month & above and in hemodynamically unstable, multi-organ dysfunction & ICU patients. • Used as an adjunct to general anesthesia in ICU patients to facilitate endotracheal intubation and mechanical ventilation. The preferred NMBAfor patients at risk for and with acute respiratory distress syndrome.

Mode of Action: Like other nondepolarizing agents, Cisatracurium binds competitively to cholinergic receptors at the motor endplate to antagonize the action of acetylcholine, resulting in blockage of neuromuscular transmission. These actions are inversed by anti-cholinesterase agents such as neostigmine or edrophonium.

Cisatracurium Besylate Injection is preferred over Atracurium Besylate Injection because:
5 times more potent & safer.Also, its higher dose is safe & efficacious.
Significantly lowers the laudanosine values making it the better choice for long term use in ICU patients. Faster recovery, without any residual muscle paralysis.

Presentation: Single-dose vial: 10mg/5ml & Multi-dose vial: 20mg/10ml

Storage: Store at a temperature between 2°C-8°C. Do not freeze.

Purpose:Tracheal intubation
Muscle relaxation during surgery
Facilitation of mechanical ventilation

Action: Blocks nerve impulses at neuromuscular junction, causing muscle paralysis

Characteristics:
Rapid onset
Intermediate duration

Metabolism: Independent of liver/kidney function, reducing risk of prolonged effects in organ impairment patients.

Additional Information:

• Delivery Time: 4-5 Weeks
• Packaging Details: Single Vial Per Box

Strength	750000 IU
Dose/Strength	7.5 Lac i.u/vial
Form	Solution
Brand	Streptokinase
Indication	Catheter occlusion
Route of Administration	Catheter directed
Usage	Emergency, ICU
Packaging Type	Vial
Manufactured By	Samarth Life Science Pvt. Ltd
Usage/Application	Hospital
Storage Instruction	COLD CHAIN

Product Name: Streptokinase for Injection
Brand Name: Stukinase
Strength: 7,50,000 IU
Packing: Single Vial Per Box

Streptokinase for injection (lyophilized) is a thrombolytic medication used to dissolve blood clots in various medical conditions. Here's a concise description with pointers:

1. Purpose: Dissolves blood clots by activating plasminogen, promoting fibrinolysis, and restoring blood flow.

2. Administration: Administered intravenously by healthcare professionals in hospital settings.

3. Mechanism of Action: Streptokinase converts plasminogen to plasmin, which breaks down fibrin in blood clots, leading to clot dissolution.

4. Indications: Used to treat acute myocardial infarction, pulmonary embolism, and arterial thrombosis.

5. Dosage: Dosage depends on the patient's weight, medical condition, and severity of thrombosis, administered as a single or divided dose.

6. Onset and Duration: Rapid onset of action within hours, with effects lasting for several days.

7. Side Effects: Common side effects may include bleeding, allergic reactions, hypotension, and fever. Risk of intracranial hemorrhage exists.

8. Contraindications: Avoid use in patients with active bleeding, recent surgery, or known hypersensitivity to streptokinase or any component of the formulation.

9. Precautions: Caution should be exercised in patients with a history of bleeding disorders, recent trauma, or gastrointestinal ulcers.

10. Storage: Store streptokinase injection according to manufacturer instructions, typically at controlled room temperature and protected from light.

11. Patient Monitoring: Continuous monitoring of vital signs, coagulation parameters, and signs of bleeding is necessary during and after administration.

12. Follow-Up: Patients should be monitored for recurrence of thrombosis and treated accordingly. Close follow-up with healthcare providers is essential for optimal management.

Additional Information:

• Packaging Details: SINGLE VIAL PER BOX

Strength	50 mg
Vial Volume	5 ml
Pack Type	Plastic Vial
Packaging Size	5ml
Packaging Type	Vial
Route	IV Infusion
Pack Size	Single Vial
Brand	Rocpure
Manufacturer	Samarth
Country of Origin	Made in India

Product Name: Rocuronium Bromide Injection 50 MG
Brand Name: Rocpure
Strength: 50 MG/ 5 ML
Packing: Single Vial Per Box
Rocuronium Bromide Injection by Samarth Pharma is a neuromuscular blocking agent used during surgical procedures to induce muscle relaxation and facilitate endotracheal intubation. This injectable medication contains rocuronium bromide, a non-depolarizing neuromuscular blocker that competitively blocks acetylcholine receptors at the neuromuscular junction, leading to temporary paralysis of skeletal muscles. Samarth Pharma ensures high-quality manufacturing standards, providing healthcare professionals with a reliable and effective solution for safe and precise muscle relaxation during surgical procedures.

Strength	100 mg
Vial Volume	10 ml
Packaging Size	10ml
Route	IV
Pack Size	Single Vial
Brand	Rocpure
Manufacturer	Samarth Life Science Pvt. Ltd.
Injection Administeration Type	IV only
Prescription/Non-Prescription	Prescription
Pack Type	Ampoule
Packaging Type	Vial

Product Name: Rocuronium Bromide Injection 100 GM
Brand Name: Ropifast
Strength: 10 ML
Packing: Single Vial Per Box

• Active Ingredient: Rocuronium bromide
• Strength: 100 mg per vial
• Form: Injectable solution
• Administration Route: Intravenous (IV) injection
• Indication: Used as a neuromuscular blocking agent to facilitate tracheal intubation and provide skeletal muscle relaxation during surgery or mechanical ventilation
• Mechanism of Action: Non-depolarizing neuromuscular blocker; competes with acetylcholine at nicotinic receptors on the motor end-plate, inhibiting neuromuscular transmission
• Dosage: Dosage varies based on the procedure, typically an initial dose of 0.6 mg/kg for intubation; maintenance doses administered as needed
• Side Effects: Hypotension, hypertension, tachycardia, injection site reactions, prolonged paralysis, allergic reactions
• Contraindications: Known hypersensitivity to rocuronium or any component of the formulation
• Precautions: Use with caution in patients with neuromuscular diseases, electrolyte imbalances, or severe renal or hepatic impairment; monitor neuromuscular function to adjust dosing
• Storage: Store in a refrigerator (2-8°C); protect from light; do not freeze

Additional Information:

• Packaging Details: Single Vial Per Box

Strength	250 mg
Packaging Size	250 mg vial
Brand	Ngmine
Packaging Type	Vial
Route of Administration	IV infusion
Usage	Hospital
Form	Lyophilized powder
Manufacturer	SAMARTH LIFE SCIENCE PVT LTD
Storage Conditions	25 degree celsius
Usage / Application	Hospital

Product Name: Bivalirudin For Injection
Brand Name: Ngmine
Strength: 250 MG
Packing: Single Vial Per Box

Description: Bivalirudin is synthetic 20 residue peptide which reversibly binds to thrombin. Thrombin is the principal enzyme of hemostasis which converts fibrinogen to fibrin and forms thrombus (Blood Clot).
Bivalirudin is a direct inhibitor of thrombin and when it binds to active site of thrombin, it cannot convert fibrinogen to fibrin and does not allow blood to clot.
Indication: Bivalirudin is indicated as an anticoagulant in adult patient undergoing per cutaneous coronary intervention (PCI), including patient with ST - Segment elevation myocardial infarction (STEMI) undergoing primary PCI. Bivalirudin is also indicated for the treatment of adult patients with unstable angina/non - ST segment elevation myocardial infarction (UA/NSTEMI) planned for urgent or early intervention. Bivalirudin should be administered with acetylsalicylic and clopidogrel.
Storage: Store below 25°C. Presentation Single vial with 10ml Ampoule of Sterile Waterfor Injection in a box. 

Additional Information:

• Packaging Details: Single Vial per Box

Packaging Size	1X10 ml Vial
Strength	10 mg/ml
Concentration	20 mg/10ml
Packaging Type	Box
Brand	Atracis
Shelf Life	18 months
Country of origin	Made in India
DRUG STRENGTH	20MG
PACK SIZE	10ML
BRAND NAME	ATRACIS

Product Name: Cisatracurium Besylate Injection
Brand Name: Atracis
Strength: 20 MG/ 10 ML
Packing: Single Vial Per Box

Cisatracurium Besylate Injection 20 MG/10 ML is a medication used as a neuromuscular blocking agent during surgeries or mechanical ventilation.

It belongs to the class of non-depolarizing neuromuscular blockers and works by competitively blocking acetylcholine receptors at the neuromuscular junction, leading to muscle relaxation.
This injection contains 20 milligrams of cisatracurium besylate per 10 milliliters and is typically administered intravenously.

Cisatracurium Besylate is commonly used to facilitate endotracheal intubation, maintain muscle relaxation during surgery, or prevent patient-ventilator asynchrony during mechanical ventilation.

Dosage and administration should be adjusted based on factors such as patient weight, age, and clinical condition.Close monitoring of neuromuscular function and respiratory status is essential during and after administration to ensure optimal patient safety and efficacy.Side effects may include prolonged muscle weakness, allergic reactions, or histamine release.

Strength	0.4 mg /ml
Packaging Size	5X1 ml Vials
Pack Type	Ampoule
Indication	Respiratory depression
Packaging Type	Vial
Brand Name	Nalox
Manufacturer	Samarth Liife Science Pvt. Ltd
Manufacturer Name	Samarth Liife Science Pvt. Ltd
Injection Routes	Intramuscular (IM), Intravenous (IV), Subcutaneous (SC)
Country of Origin	Made in India

Product Name: Naloxone Injection IP
Brand Name: Nalox
Strength:0.4 MG/1 ML
Packing: 5 Ampoules Per Box

_{Product Description:}

NALOX 0.4 mg Injection is a fast-acting opioid antagonist used to reverse the life-threatening effects of opioid overdose, including respiratory depression, sedation, and hypotension. It binds competitively to opioid receptors in the central nervous system, displacing opioids like morphine, heroin, fentanyl, and others.

This life-saving antidote is vital in emergency settings, hospitals, ambulances, and can also be part of take-home kits for high-risk opioid users under proper medical guidance.

_Indications:

NALOX (Naloxone Injection 0.4 mg/mL) is indicated for:

• Emergency treatment of known or suspected opioid overdose

• Reversal of opioid-induced respiratory and CNS depression

• Postoperative opioid reversal in clinical settings

• Neonatal opioid-induced respiratory depression

Additional Information:

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

Strength	0.2 mg/ml
Vial Volume	1 ml
Pack Type	Ampoule
Brand	LICOLATE
Manufacturer	Samarth Life Science Pvt. Ltd Sciences Pvt Ltd
Pack Size	1 ml
Country of Origin	Made in India

Product Name: Glycopyrrolate Injection IP
Brand Name: Licolate
Stregth:0.2 MG/ 1 ML 
Packing:10 Ampoules Per Box

• Medication Type: Glycopyrrolate Injection
• Purpose: Used to reduce saliva, mucus, and stomach acid secretion during surgical procedures or for certain medical conditions
• Administration: Typically administered intravenously or intramuscularly
• Mechanism of Action: Anticholinergic agent that blocks acetylcholine receptors, reducing secretions
• Indications: Used to control excessive secretions in surgery, manage drooling in neurological conditions, and treat peptic ulcers
• Dosage Strength: Available in vials or prefilled syringes with varying concentrations
• Side Effects: Common side effects include dry mouth, blurred vision, and urinary retention
• Monitoring: Healthcare providers may monitor for adverse reactions, especially in patients with pre-existing conditions such as glaucoma or urinary retention.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 Weeks
• Packaging Details: 10 Ampoules Per Box

Strength	5000 IU
Dosage/Strength	5 ml
Brand	CAPRIN
Manufacturer Name	Samarth Life Sciences Pvt Ltd
Pack Size	10 Vials
Manufactured By	Samarth Life Sciences Pvt Ltd
Heparin Sodium IP	Heparin Injetion
Packaging Type	Vial

Product Name: Heparin Sodium Injection 
Brand Name: Caprin
Strength: 5,000 IU/ 5 ML
Packing: Single Vial Per Box

Product Description

Caprin (Heparin Sodium Injection 5,000 IU/5 mL) by Genex Pharma is a sterile, preservative-free anticoagulant solution designed for both therapeutic and prophylactic use. Heparin is a fast-acting, naturally occurring anticoagulant that prevents the formation and extension of blood clots by potentiating the activity of antithrombin III. Caprin is widely used in hospitals for the management of thromboembolic disorders and as an adjunct in cardiovascular and extracorporeal procedures.

Indications

Caprin is indicated for:

 

• Prophylaxis and treatment of venous thrombosis and pulmonary embolism

• Prevention of clotting during extracorporeal circulation (e.g., open-heart surgery, renal dialysis)

• Adjunct therapy in the treatment of myocardial infarction, unstable angina, and other thromboembolic conditions

• Maintenance of patency in indwelling intravenous catheters (when used in appropriate dilution)

Storage

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

• Protect from light and freezing

• Keep out of reach of children

Additional Information:

• Production Capacity: 1000
• Packaging Details: A Single Vial Per Box

Strength	8.4 %
Vial Volume	25 ml
Container Type	Vial
Manufacturer	Samarth Life Sciences Pvt Ltd
Pack Size	25 ml
Route	IV
Grade	IP
Usage Type	Human
Prescription/Non prescription	Prescription
Composition	8.4% W/V,25ML
Brand Name	SODABICARB
Shelf Life	24 Months
Pack Type	Vial
Prescription/Non-Prescription	Prescription
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Brand	SODABICARB

Product Name: Sodium Bicarbonate Injection IP
Brand Name: Sodabicarb
Strength: 8.4 % W/V,25 ML
Packing: 5 Ampoules Per Box

Sodium bicarbonate injection is a medication used to treat acidosis and certain other conditions by neutralizing excess acid in the body. Here's a concise description with pointers:

1. Purpose: Treats metabolic acidosis, severe dehydration, and certain drug overdoses by neutralizing excess acid in the body.

2. Administration: Administered intravenously by healthcare professionals, typically in a hospital or emergency setting.

3. Mechanism of Action: Sodium bicarbonate acts as a buffer, neutralizing acid by combining with hydrogen ions to form water and carbon dioxide.

4. Indications: Used in cases of severe metabolic acidosis, such as diabetic ketoacidosis or renal failure, and in certain drug intoxications.

5. Dosage: Dosage varies based on the patient's condition and blood pH level, administered slowly to avoid rapid changes in pH.

6. Onset and Duration: Rapid onset of action, with effects lasting for a relatively short duration.

7. Side Effects: Common side effects may include metabolic alkalosis, electrolyte imbalances, and tissue irritation at the injection site.

8. Contraindications: Avoid use in patients with alkalosis, hypocalcemia, or heart failure, and in those with hypersensitivity to sodium bicarbonate.

9. Precautions: Care should be taken in patients with impaired kidney function or congestive heart failure, as sodium bicarbonate can exacerbate fluid overload.

10. Storage: Store sodium bicarbonate injection according to manufacturer instructions, typically at controlled room temperature and protected from light.

11. Patient Monitoring: Continuous monitoring of blood pH, electrolytes, and vital signs is essential during administration to ensure proper dosing and prevent complications.

12. Education: Healthcare providers should educate patients and caregivers on the purpose of the medication, potential side effects, and the importance of adherence to treatment protocols.

Additional Information:

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

Concentration	99.9%
Packaging Size	250ml
Pack Volume	250 ml
Bottle Type	Clear Glass
Strength	10%
Usage	Inhalation
Grade	IP
Brand	SEVFURANE-50
Packaging Type	Glass bottle
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Prescription/Non-Prescription	Prescription
Country of Origin	Made in India
Brand Name	Sevfurane-250
Manufactured By	Samarth Life Science Pvt. Ltd
Packing Type	Single Bottle per Box
Dose Strength	250 ml

Sevoflurane Liquid for Inhalation (SEVFURANE-250 250 mL)

1. Brand Name: SEVFURANE-250 
2. Composition: Sevoflurane 250 mL
3. Form: Inhalation Liquid
4. Therapeutic Use: Anesthetic agent used for induction and maintenance of general anesthesia
5. Mechanism of Action: Sevoflurane acts on the central nervous system by enhancing inhibitory neurotransmission and suppressing excitatory neurotransmission, resulting in a reversible state of general anesthesia.
6. Indications:
   • Induction and maintenance of general anesthesia in adult and pediatric patients
   • Used in surgeries requiring controlled and reversible anesthesia
7. Dosage: Administered via inhalation by anesthesia professionals, with the dose adjusted based on the patient’s age, weight, and clinical condition.
8. Packaging: Single bottle of 250 mL per box
9. Shelf Life: 24 months from manufacturing date
10. Storage Conditions: Store below 30°C, protect from light.
11. Key Features:

• Quick onset and rapid recovery from anesthesia
• Low blood-gas solubility, ensuring fast induction and emergence
• Suitable for a wide range of surgical procedures

Additional Information:

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

Vial Volume	20 ml
With Dextrose	With Dextrose
Packaging Size	20 ml
Route	Infiltration
Pack Type	Ampoule
Brand	Ropifast
Brand Name	ROPIFAST
Manufacturer	Samarth Life Science Pvt. Ltd
Packaging Type	SINGLE AMPOULE PER BOX
Usage	For surgical and pain management procedures
Prescription/Non prescription	Prescription
Country of Origin	Made in India
Strength	0.2%, 20 ML
Storage	Store at controlled room temperature (15 DegreeC to 30 DegreeC).
Uses	Ropivacaine is used for local anesthesia, Arrhythmia, piles and mouth ulcers.
Work	Ropivacaine is a local anesthetic. It works by blocking the transmission of pain signals from the ne
Advantages	Provides long-lasting pain relief with reduced motor impairment compared to other anesthetics.
Packing	Single Ampoules Per Box
Medical Use	Administered for local or regional anesthesia to numb specific areas of the body during surgical pro
Used	Single Used Only
Composition	Ropivacaine Hydrochloride (equivalent to Ropivacaine base) Water for Injection

Product Name: Ropivacaine Injection IP 20 MG/ML
Brand Name: Ropifast
Strength: 0.20 %
Packing: Single Ampoules Per Box

Ropivacaine Injection IP 20 MG/ML is a local anesthetic used primarily for surgical procedures and pain management. Here's a concise overview with pointers:

Medical Use: Administered for local or regional anesthesia to numb specific areas of the body during surgical procedures or for postoperative pain management.

Mechanism of Action: Belongs to the amide group of local anesthetics, working by blocking nerve impulses at the site of injection, resulting in temporary loss of sensation.

Dosage Strength: Each milliliter of solution contains 20 mg of Ropivacaine, providing a standardized dose for injection.

Onset of Action: Rapid onset of action allows for quick pain relief, making it effective for both short and long procedures.

Medical Supervision: Administration requires skilled healthcare professionals due to potential adverse reactions, including systemic toxicity and nerve damage.

Side Effects: Common side effects may include numbness, tingling, and temporary weakness in the injected area. Rare but severe side effects such as cardiac toxicity may occur with systemic absorption.

Contraindications: Avoid in patients with known hypersensitivity to ropivacaine, severe hepatic impairment, or those with a history of cardiac conduction disturbances.

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.

Ropivacaine Injection IP 20 MG/ML is a valuable tool in anesthesia and pain management, providing effective and targeted relief while minimizing systemic side effects.

Additional Information:

• Item Code: 8965
• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: SINGLE AMPOULE PER BOX

Strength	7.5 %, 20 ML
Vial Volume	20 ml
With Dextrose	Plain
Dose	0.75%, 20 ML
Route	Infiltration
Pack Type	Glass Vial
Packaging Size	20ML
Brand	ROPIFAST
Brand Name	ROPIFAST
Manufacturer	Samarth Lifesciences
Packaging Type	0.75%, 20 ML

Product Name: Ropivacaine Injection IP
Brand Name: Ropifast
Strength: 0.75 MG/ML
Packing: Single Ampoules Per Box

Ropivacaine Hydrochloride Injection 0.75 MG/ML is a local anesthetic primarily used for surgical anesthesia and postoperative pain management. Here's a concise overview with pointers:

Medical Use: Administered for local or regional anesthesia to numb specific areas of the body during surgical procedures or for postoperative pain relief.

Mechanism of Action: Belongs to the amide group of local anesthetics, working by blocking nerve impulses at the site of injection, resulting in temporary loss of sensation.

Dosage Strength: Each milliliter of solution contains 0.75 mg of Ropivacaine Hydrochloride, providing a standardized dose for injection.

Onset of Action: Rapid onset of action allows for quick pain relief, making it effective for both short and long procedures.

Medical Supervision: Administration requires skilled healthcare professionals due to potential adverse reactions, including systemic toxicity and nerve damage.

Side Effects: Common side effects may include numbness, tingling, and temporary weakness in the injected area. Rare but severe side effects such as cardiac toxicity may occur with systemic absorption.

Contraindications: Avoid in patients with known hypersensitivity to ropivacaine, severe hepatic impairment, or those with a history of cardiac conduction disturbances.

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.

Ropivacaine Hydrochloride Injection 0.75 MG/ML is a valuable agent in anesthesia and pain management, providing effective and targeted relief while minimizing systemic side effects.

Additional Information:

• Packaging Details: SINGLE AMPOULE PER BOX

Strength	50 mg/5 ml
Packaging Type	Box of 5x5x5 ml
Brand	PROTA
Indication	Cardiac surgery
Route of Administration	IV slow
Usage	OT
PACKAGING SIZE	25 AMOULES PER BOX
DRUG STRENGTH	50MG
BRAND NAME	PROTA
FORM	INJECTION

Product Name: Protamine Sulphate Injection 
Brand: Prota
Strength: 50 MG
Packing: 25 Ampoules Per Box

Product Description:

PROTA (Protamine Sulphate Injection 50 mg) by Genex Pharma is a sterile, preservative-free solution used to neutralize the anticoagulant effects of heparin. It is especially vital during cardiac surgeries, dialysis, or other procedures where heparin is used and needs to be reversed quickly and safely. PROTA is manufactured under strict quality standards to ensure efficacy, purity, and safety in critical care settings.

Composition (Per 5 mL vial):

 

• Protamine Sulphate – 50 mg (10 mg/mL)

• Water for Injection – q.s.

• pH adjusted with hydrochloric acid and/or sodium hydroxide

Mechanism of Action:

Protamine sulphate is a highly alkaline, positively charged polypeptide that combines with negatively charged heparin to form a stable, inactive complex. This action neutralizes heparin’s anticoagulant effect almost immediately, making it essential in reversing heparin-induced bleeding during and after surgery.

Indications:

 

• To neutralize the anticoagulant effect of heparin after surgery or hemodialysis

• Reversal of heparin in cases of heparin overdose or toxicity

• Used in cardiac surgeries, vascular procedures, or other operations involving extracorporeal circulation

• Emergency management of bleeding complications due to heparin

Additional Information:

• Packaging Details: Box

Strength	60 mg
Brand	Lowcap
Form	Prefilled Syringe
Pack Type	Box
Volume	0.6 ml
Salt Type	Enoxaparin sodium
Pack Size	0.6 ml
Brand Name	LOWCAP
Manufacturer	samarth life science Pvt. Ltd
Prescription/ Non Prescription	Prescription
Packaging Type	Pre filled syringe
Also Gives	PCD Pharma Franchise
Country of Origin	Made in India

Product Name: Enoxparin Sodium Injection
Brand Name: Lowcap
Strength: 60 MG/ 0.6 ML
Packing: Single PFS Per Box

Description:

Lowcap (Enoxaparin Sodium Injection 60 mg/0.6 mL) is a low molecular weight heparin (LMWH) used for the prevention and treatment of thromboembolic disorders. It has a more predictable anticoagulant response than unfractionated heparin and a longer half-life, allowing for once or twice daily dosing. Enoxaparin works by inhibiting Factor Xa and, to a lesser extent, Factor IIa (thrombin), preventing clot formation.

Composition (per pre-filled syringe of 0.6 mL):

• Enoxaparin Sodium equivalent to 60 mg of anhydrous Enoxaparin

• Water for Injection: q.s.

Mechanism of Action:

Enoxaparin enhances the inhibition of Factor Xa through antithrombin III, leading to decreased thrombin generation and clot formation. It exhibits a higher anti-Factor Xa to anti-Factor IIa activity ratio (~3.8:1), which contributes to a lower risk of bleeding and a more stable anticoagulant effect compared to unfractionated heparin.

Indications:

• Prophylaxis of deep vein thrombosis (DVT) in surgical or medical patients

• Treatment of DVT, with or without pulmonary embolism

• Unstable angina and non-ST elevation myocardial infarction (NSTEMI)

• STEMI (in combination with thrombolytics or PCI)

• Prevention of thrombus formation in extracorporeal circuits (e.g., during hemodialysis)

Dosage & Administr

Additional Information:

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

Strength	100mg/10ml
Vial Volume	10 ml
Pack Type	Ampoule
Packaging Size	10ml
Route	IV
Pack Size	Single Vial
Brand	Atrapure
Manufacturer	Samarth
Country of Origin	Made in India

Product Name: Atracurium Besylate Injection
Brand Name: Atrapure
Strength: 100 mg/ 10 ml
Packing:Single Vial Per Box

ATRAPURE (Atracurium Besylate Injection 100 mg/10 mL) is a non-depolarizing skeletal muscle relaxant intended for intravenous use. It is designed to facilitate endotracheal intubation, produce skeletal muscle relaxation during surgery, and support controlled ventilation in intensive care settings. With a well-established safety profile, ATRAPURE provides rapid onset, intermediate duration of action, and organ-independent metabolism—making it a preferred choice in both surgical and critical care environments.

Composition:

Each 10 mL vial contains:

• Atracurium Besylate equivalent to Atracurium 100 mg (10 mg/mL)

• Water for Injection IP q.s.

• pH adjusted with Benzenesulfonic acid

Indications:

• Facilitation of endotracheal intubation

• Induction and maintenance of skeletal muscle relaxation during surgery

• Control of muscle tone in mechanically ventilated patients in ICUs

Key Features of ATRAPURE 100 mg/10 mL:

• Rapid onset and intermediate duration for procedural flexibility

• Metabolized independently of liver or kidney function

• Ideal for surgeries, intubation, and mechanical ventilation

• Stable, GMP-compliant formulation with consistent clinical performance

Strength	10 MG /1 ML
Packaging Type	Box
Packaging Size	Single Ampoules Per Box
Brand	FRENIN
Country of Origin	Made in India
Also gives	PCD Pharma Franchise, Third Party Manufacturing
Manufactured By	Samarth Life Sciences Pvt Ltd.

Product Name: Phenylephrine Injectection IP
Brand Name: Frenin
Strength: 10 MG/ 1ML
Packing: Single Ampoule Per Box

Description:

Frenin contains Phenylephrine Hydrochloride, a potent alpha-1 adrenergic receptor agonist used primarily as a vasopressor. It acts by causing vasoconstriction, leading to an increase in blood pressure, making it a vital drug in emergency medicine and anesthesia.

Indications:Hypotension during anesthesiaShock (including septic or neurogenic shock)Vasodilatory hypotensionAdjunct in cardiopulmonary resuscitation (CPR)As a mydriatic agent (off-label)Storage:

Store below 25°C. Protect from light. Do not freeze.
For single use only.

Key Features of Frenin by Genex Pharma:

 

• Rapid and effective management of anesthesia-induced hypotension

• High-purity formulation for reliable hemodynamic control

• Manufactured in WHO-GMP certified facilities for maximum safety and quality assurance

Additional Information:

• Production Capacity: 1000
• Delivery Time: 5-6 WEEKS
• Packaging Details: SINGLE AMPOULE PER BOX

Strength	25000 IU
Packaging Size	5 ml
Brand	CAPRIN
Packaging Type	10 VIALS PER BOX
Manufacturer Name	SAMARTH LIFESCIENCES
Prescription/ Non Prescription	Prescription
Usage	Treatment and prevention of blood clots

Product Name: Heparin Sodium Injection
Brand Name: Caprin
Strength: 25000 IU
Packing: 10 Vial Per Box


Product Description:

Caprin (Heparin Sodium Injection 25,000 IU) is a high-potency anticoagulant formulation used for the prevention and treatment of thromboembolic disorders. It contains Heparin Sodium, a fast-acting, naturally occurring anticoagulant derived from porcine intestinal mucosa. It acts by inhibiting clotting factors IIa (thrombin) and Xa via antithrombin III, thus preventing the formation and propagation of blood clots.

Composition (per 5 mL vial):

• Heparin Sodium IP: 25,000 IU

• Water for Injection: q.s.

• Benzyl Alcohol (as preservative): 1% v/v (if applicable – check packaging)

Packaging Type	Ampoule
Brand	Aldopam
Salt Form	Chloride
Packaging Size	20 ml
Usage/Application	Hospital
Injectable Form	Liquid
Strength	500mg/20ml
Brand name	Aldopam
Pack type	3 Ampoules per box
manufactured in	India
manufactured by	Samarth Life Sciences Pvt. Ltd.

Alodpam used as Detoxifying agents, antidotes - Poisoning, Toxicity Indication: Pralidoxime lodide Injection (P.A.M.) is indicated as an antidote: In the treatment of poisoning due to those pesticides and chemicals of the organophosphate class which have anticholinesterase activity,In the control of overdosage by anticholinesterase medicine used in the treatment of myasthenia gravis Packages:Aldopam supplied as Pam Injection 500 mcg/20 ml, 20 ml of 2 ampoules per Boxes

Additional Information:

• Item Code: Aldopam
• Production Capacity: 1000
• Delivery Time: 3-4 Weeks
• Packaging Details: A Single Vial Per Box

Strength	250 mg
Pack Size	2 Ampoules
Brand	DOBUSTAT
Pack Type	Vial
Composition	Dobutamine
Form	Infusion
Packaging Type	Ampoule
Brand Name	Dobustat
Manufactured By	Samarth Lifesciences
Grade Standard	Medicine Grade
Country of Origin	Made in India

Dobutamine is a sympathomimetic drug used in the treatment of heart failure and cardiogenic shock. Its primary mechanism is direct stimulation of β 1 receptor of the sympathetic nervous system.

 

Indication:

 

Dobutamine is indicated when parenteral therapy is necessary for inotropic support in the short- term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures.

 

Packages:

 

Dobustat suplied as

• Dobutamine 250 Mg/5Ml 2 ampoules of 5 ml Per Boxes

• Dobutamine Injection 250mg/20 ml single Vial Per Boxes.

Additional Information:

• Item Code: Dobustat

Dose/Strength	500 mg
Packaging Size	5 ml
Brand	TRANEMIC
Strength	500mg/5ml
Packaging Type	Box
Usage	Surgery bleed
Route of Administration	IV infusion
Prescription Type	Prescription
Manufactured By	Samarth Life Sciences Pvt Ltd

Product Name: Tranexamic Acid Injection IP
Brand Name: Tranemic
Strength: 500 MG / 5 ML
Packing: 25 Ampoules Per Box

Tranexamic Acid Injection IP is a medication primarily used to control or prevent excessive bleeding, particularly in surgical and trauma settings. Here's a concise overview with pointers:

Medical Use: Administered to manage or prevent significant blood loss during surgical procedures, trauma, or conditions such as menorrhagia (heavy menstrual bleeding).

Mechanism of Action: Works by inhibiting the breakdown of blood clots, preventing the dissolution of fibrin and stabilizing blood clots, thereby 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 makes it effective in controlling bleeding during surgical procedures or trauma.
Medical Supervision: Administration should be under the supervision of healthcare professionals, 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 or hypersensitivity reactions may occur.

Contraindications: Avoid in patients with a history of thromboembolic events, renal impairment, or hypersensitivity to tranexamic 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.

Tranexamic Acid Injection IP is a vital tool in managing bleeding disorders, providing rapid and effective control of hemorrhage in various clinical settings.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 5-6 WEEKS
• Packaging Details: 25 AMPOULES PER BOX

Strength	20 Units/ml
Pack Size	1 ml
Pack Type	Ampoule
Packaging Size	1 ml
Usage	Operation theatre
Route of Administration	IV infusion
Formulation Type	Concentrate
Medicine Type	Injection
Usage/Application	Hospital
Manufacturer	samarth Life Science Pvt Ltd
Brand	Samarth Life Sciences Pvt Ltd
Country of Origin	Made in India

Product Name: Vasopressin Injection
Brand Name: Cpressin P
Strength: 20 IU/1 ML
Packing: Single PFS Per Box

Vasopressin Injection is a medication primarily used to manage certain medical conditions such as diabetes insipidus, cardiac arrest, and septic shock. Here's a concise overview with pointers:

• Medical Use: Administered to treat diabetes insipidus by reducing excessive urination and to manage cardiac arrest or septic shock by increasing blood pressure.

• Mechanism of Action: Mimics the action of the natural hormone vasopressin (antidiuretic hormone), which regulates water reabsorption in the kidneys and promotes vasoconstriction, leading to increased blood pressure.

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

• Onset of Action: Rapid onset of action makes it effective in managing acute conditions such as cardiac arrest or severe hypotension.

• Medical Supervision: Administration should be under the supervision of healthcare professionals, as dosing and monitoring are critical to prevent complications such as excessive vasoconstriction or water retention.

• Side Effects: Common side effects may include nausea, vomiting, and headache. Excessive vasoconstriction may lead to tissue ischemia or infarction.

• Contraindications: Avoid in patients with known hypersensitivity to vasopressin, coronary artery disease, or certain cardiac arrhythmias.

• 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.

Vasopressin Injection plays a crucial role in managing various medical emergencies, providing rapid stabilization of blood pressure and fluid balance in critical situations.

Additional Information:

• Packaging Details: Single PFS Per Box

Strength	40 Unit
Pack Size	1 ml
Pack Type	Ampoule
Usage	Operation theatre
Route of Administration	IV infusion
Formulation Type	Liquid
Medicine Type	Injection
Manufacturer	Samarth Life Science Pvt Ltd
Brand	Cpressin
Product Name	Vasopressin Injection
Packing	Single PFS Per Box

Product Name: Vasopressin Injection 
Brand Name: Cpressin
Strength: 40 IU/ 1 ML
Packing: Single PFS Per Box

Vasopressin Injection 40 IU/1 ML is a medication used to manage conditions like diabetes insipidus, cardiac arrest, and septic shock. Here's a concise overview with pointers:

• Medical Use: Administered to treat diabetes insipidus by reducing excessive urination and to manage cardiac arrest or septic shock by increasing blood pressure.

• Mechanism of Action: Mimics the action of vasopressin (antidiuretic hormone), regulating water reabsorption in the kidneys and promoting vasoconstriction, leading to increased blood pressure.

• Dosage Strength: Each milliliter of solution contains 40 International Units (IU) of vasopressin, providing a standardized dose for injection.

• Onset of Action: Rapid onset of action allows for quick management of acute conditions such as cardiac arrest or severe hypotension.

• Administration: Typically administered intravenously or intramuscularly, ensuring rapid delivery and onset of action.

• Medical Supervision: Administered under the supervision of healthcare professionals to monitor dosing and prevent complications such as excessive vasoconstriction or water retention.

• Side Effects: Possible side effects include nausea, vomiting, and headache. Excessive vasoconstriction may lead to tissue ischemia or infarction.

• Contraindications: Avoid in patients with known hypersensitivity to vasopressin, coronary artery disease, or certain cardiac arrhythmias.

• 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.

Vasopressin Injection 40 IU/1 ML is a critical medication in managing various medical emergencies, providing rapid stabilization of blood pressure and fluid balance in critical situations.

Additional Information:

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

Concentration	99.9%
Packaging Size	50ml
Pack Volume	50ML
Bottle Type	Clear Glass
Usage	Inhalation
Grade	IP
Brand	Sevoflurane
Packaging Type	Glass bottle
Country of Origin	Made in India
Brand Name	Sevfurane 50

Product Name: Sevoflurane Liquid For Inhalation
Brand Name: Sevfurane 50
Strength: 50 ML
Packing: Single Bottle Per Box

• Sevoflurane Liquid For Inhalation 50 ML is a potent inhalation anesthetic commonly used to induce and maintain general anesthesia during surgical procedures.
• This formulation is intended for inhalation administration through specialized vaporizers, allowing for precise control over anesthesia depth.
• Sevoflurane belongs to the halogenated ether class of anesthetics and works by depressing the central nervous system.
• Packaged in a 50 milliliter container, this liquid formulation of sevoflurane is vaporized into a gas before being inhaled by the patient.
• Its rapid onset and offset of action make sevoflurane an attractive choice for anesthesia management, enabling quick adjustments during procedures.
• Proper dosage and administration should be supervised by trained anesthesia professionals to ensure patient safety and optimal anesthesia depth.
• Potential side effects may include respiratory depression, hypotension, and postoperative nausea and vomiting.
• Due to its flammable nature, sevoflurane should be handled and stored with caution, away from heat sources.

Additional Information:

• Packaging Details: SINGLE BOTTLE PER BOX

Packaging Type	Vial
Strength	4MG/2ML
Volume Per Ampoule	2 ml
Manufacturer	Samarth Life Scinces Pvt Ltd
Brand	ADRENOR
Shelf Life	18 months
Storage Conditions	Below 25 Degree C
Packaging Size	20 ampoules per box
Usage/Application	Clinical
Country of Origin	Made in India

Product Name: Noradrenaline Bitartrate Injection
Brand Name: Adrenor
Strength: 4 MG/ 2 ML
Packing: 20 Ampoules Per Box

Noradrenaline Bitartrate Injection 4 mg / 2 ml is a medication used to manage acute hypotension and shock. Here's a concise overview with pointers:

Medical Use: Administered to treat acute hypotension and shock by increasing blood pressure and improving perfusion to vital organs.

Mechanism of Action: Acts as a potent vasoconstrictor by stimulating alpha-adrenergic receptors, leading to increased systemic vascular resistance and blood pressure.

Dosage Strength: Each 2 ml ampoule contains 4 mg of Noradrenaline Bitartrate, providing a standardized dose for intravenous administration.

Onset of Action: Rapid onset of action allows for prompt correction of hypotension, making it valuable in critical situations.

Medical Supervision: Administration requires close monitoring by healthcare professionals due to potential hemodynamic effects, including hypertension and tissue ischemia.

Side Effects: Common side effects may include hypertension, arrhythmias, and tissue necrosis if extravasation occurs.

Contraindications: Avoid in patients with severe hypertension, ventricular tachycardia, or hypovolemia unresponsive to fluid replacement.

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.

Noradrenaline Bitartrate Injection 4 mg / 2 ml provides rapid correction of hypotension and shock, aiding in the stabilization of critically ill patients.

Additional Information:

• Production Capacity: 1000
• Delivery Time: 4-5 weeks
• Packaging Details: 20 AMPOULES PER BOX

Strength	100 mg
Pack Size	100 ml
Brand	PARAFUSE
Pack Type	Bottle
Usage	Paediatric
Drug Composition	Paracetamol 100mg
Packaging Type	Bottle
Route	IV
Manufacturer	Samarth Life Sciences Pvt Ltd
Also Gives	PCD Pharma Franchise

Product Name: Paracetamol Injection
Brand Name: Parafuse
Strength: 10 MG/1 ML
Packing: Single Bottle Per Box

Product Overview

Parafuse (Paracetamol Infusion) 10 mg/1 mL is a sterile, ready-to-use intravenous formulation of Paracetamol (Acetaminophen). It provides rapid and effective relief of pain and fever, making it an essential option in both adult and pediatric patients where oral or rectal administration is not feasible. With its predictable pharmacological profile and excellent tolerability, Parafuse is widely used in hospitals for acute pain management and perioperative care.

Indications

Parafuse is indicated for:

• Fever (Pyrexia): Reduction of elevated body temperature in adults and children.

• Mild to Moderate Pain Relief: Headache, musculoskeletal pain, dental pain, and postoperative pain.

• Adjunct in Severe Pain: Combined with opioid analgesics to reduce opioid requirement.

• Perioperative Pain Management: Effective in surgical and critical care settings where oral therapy is unsuitable.

Key Benefits

• Rapid onset of action with effective fever and pain control.

• Well tolerated with minimal gastrointestinal side effects compared to NSAIDs.

• Opioid-sparing effect in severe pain management.

• Suitable for patients unable to take oral or rectal medications.

Storage

• Store below 25°C.

• Protect from light.

• Do not freeze.

• Keep out of reach of children.

Additional Information:

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

Strength	40 mg
Brand	ZEROKLOT
Form	Prefilled Syringe
Pack Type	Box
Volume	0.4 ml
Salt Type	Enoxaparin sodium
Pack Size	0.4 ml
Brand Name	ZEROKLOT
Manufacturer	SAMARATH LIFE SCIENCE PVT. LTD
Packaging Type	Pre filled syringe

Product Name: Enoxaparin Sodium Injection 
Brand Name: Zeroklot
Strength: 40 MG/0.4 ML
Packing: Single PFS Per Box

1. Purpose: Prevents blood clots in conditions such as deep vein thrombosis (DVT), pulmonary embolism (PE), and during certain medical procedures like surgery.

2. Mechanism of Action: It works by inhibiting clot formation, particularly by blocking factor Xa, a key component in the clotting cascade.

3. Administration: Administered subcutaneously (under the skin) usually once or twice daily, depending on the indication and patient's condition.

4. Dosage: Dosage varies depending on the individual's weight, medical condition, and the indication for use.

5. Monitoring: Regular monitoring of blood coagulation parameters, such as activated partial thromboplastin time (aPTT) or anti-factor Xa levels, may be necessary in certain cases to ensure appropriate dosing.

6. Adverse Effects: Common side effects include bleeding, bruising at the injection site, and thrombocytopenia (low platelet count).

7. Contraindications: Should not be used in patients with active major bleeding, severe thrombocytopenia, or hypersensitivity to enoxaparin or its components.

8. Special Populations: Dosing adjustments may be needed in patients with renal impairment or those who are pregnant.

9. Drug Interactions: Enoxaparin can interact with other medications, particularly those affecting blood clotting, and should be used cautiously with such drugs.

10. Storage: Store at controlled room temperature and protect from light. Do not freeze.

Additional Information:

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

Strength	25mg/2.5ml
Vial Volume	2.5 ml
Packaging Size	2.5ml
Route	IV
Pack Size	Single Vial
Brand	ATRAPURE
Manufacturer	SAMARTH LIFE SCIENE PVT.LTD
Prescription/Non-Prescription	Prescription
Packaging Type	Vial
Pack Type	Ampoule

Product Name: Atracurium Besylate Injection IP 
Brand Name: Atrapure
Strength: 25 MG/ 2.5 ML
Packing: 

• Medication Type: Atracurium besylate injection is a neuromuscular blocking agent used during surgical procedures to induce muscle relaxation.
• Purpose: Administered to facilitate endotracheal intubation, provide muscle relaxation during surgery, and improve surgical conditions.
• Mechanism of Action: Acts as a non-depolarizing neuromuscular blocker by competitively inhibiting the action of acetylcholine at the neuromuscular junction, leading to muscle paralysis.
• Indications: Used in anesthesia to achieve skeletal muscle relaxation, particularly for procedures requiring controlled ventilation.
• Dosage: Administered intravenously by healthcare professionals based on patient's weight, age, and the desired level of muscle relaxation.
• Onset of Action: Exhibits rapid onset of action, with effects typically observed within 2 to 3 minutes after administration.
• Duration of Action: Provides intermediate duration of muscle relaxation, lasting approximately 20 to 35 minutes.
• Side Effects: Common side effects may include hypotension, tachycardia, bronchospasm, and histamine release. Bradycardia and prolonged muscle weakness are potential adverse reactions.
• Precautions: Patients with preexisting cardiovascular or respiratory conditions should be closely monitored during administration. Dosage adjustments may be necessary in patients with impaired renal or hepatic function.
• Storage: Store the injection as per manufacturer's instructions, typically at room temperature away from light and moisture.
• Availability: Available by prescription and administered under the supervision of anesthesiologists or trained healthcare professionals in operating rooms or intensive care units.

Strength	50 mg
Packaging Type	SINGLE AMPOULE PER BOX
Pack Type	Vial
Packaging Size	1 mL
Brand Name	Fenoxene
Manufacturer Name	samarth life science Pvt. Ltd

Product Name: Phenoxyenzamine Hydrochloride Injection
Brand Name: Fenoxene
Strength: 50 MG/ 1 ML
Packing: Single Ampoule Per Box

Phenoxybenzamine Hydrochloride Injection 50 MG/1 ML is a medication primarily used in the management of conditions such as pheochromocytoma and certain forms of hypertension. Here's a concise overview with pointers:

• Medical Use: Administered to manage conditions such as pheochromocytoma, a tumor of the adrenal gland, and certain forms of hypertension by blocking alpha-adrenergic receptors, leading to vasodilation and blood pressure reduction.

• Mechanism of Action: Acts as a non-selective alpha-adrenergic antagonist, inhibiting the effects of catecholamines such as adrenaline and noradrenaline on smooth muscle, resulting in vasodilation and decreased blood pressure.

• Dosage Strength: Each 1 ml ampoule contains 50 mg of Phenoxybenzamine Hydrochloride, providing a standardized dose for intravenous or intramuscular administration.

• Onset of Action: Rapid onset of action allows for quick reduction of blood pressure, making it valuable in hypertensive emergencies.

• Medical Supervision: Administration requires close monitoring by healthcare professionals due to potential hemodynamic effects, including hypotension and reflex tachycardia.

• Side Effects: Common side effects may include orthostatic hypotension, dizziness, and nasal congestion. Careful monitoring is necessary to mitigate potential adverse reactions.

• Contraindications: Avoid in patients with hypersensitivity to phenoxybenzamine, congestive heart failure, or impaired renal function.

• 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.

Phenoxybenzamine Hydrochloride Injection 50 MG/1 ML is an essential medication in the management of pheochromocytoma and certain forms of hypertension, providing rapid blood pressure reduction and symptomatic relief in critical situations.

Additional Information:

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

Strength	0.5%
Vial Volume	20 ml
With Dextrose	With Dextrose
Packaging Size	20ml
Packaging type	Vial
Uses	As local anesthesia
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Prescription/Non-Prescription	Prescription
Country of Origin	Made in India

Product Name: Bupivacaine Injection
Brand Name: Numbcaine
Strength: 0.5 %,20 ml
Packing: Single Vial Per Box

Description:

NUMBCAINE 0.5% is a sterile, preservative-free solution of Bupivacaine Hydrochloride 0.5% w/v, specially formulated for use as a local and regional anesthetic. Manufactured by Genex Pharma, this product is intended for epidural, spinal, and peripheral nerve block anesthesia in both surgical and obstetric applications.

Each 20 mL vial delivers consistent potency and long-lasting anesthetic effects, making it a trusted choice for healthcare professionals across hospitals, operation theatres, and clinics.

Benefits of NUMBCAINE (by Genex Pharma):

• High quality manufacturing ensures patient safety and clinical reliability

• Long-acting effect for prolonged procedures and postoperative pain relief

• Stable formulation with consistent anesthetic efficacy

• Trusted brand: Genex Pharma is known for its robust quality control and injectable expertise

Storage Conditions:

 

• Store below 25°C

• Protect from light and freezing

• Use under strict medical supervision

Additional Information:

• Delivery Time: 4-5 weeks
• Packaging Details: A Single Vial Per Box

Strength	25 mg
Packaging Size	5 ml
Packaging Type	Vial
Brand	NITROCIN
Manufacturer	Samarth Life Science Pvt. Ltd.
Country of Origin	Made in India

Porduct Name: Nitroglycerin Injection IP 25 MG
Brand Name: Nitrocin
Strength: 25 MG/ 5 ML
Packing:Single Vial Per Box

Nitroglycerin Injection 25 MG/10 ML is a medication primarily used to manage acute angina pectoris and congestive heart failure. Here's a concise overview of its key features:

• Medical Use: Nitroglycerin Injection 25 MG/10 ML is administered to relieve chest pain associated with angina and reduce preload in congestive heart failure.

• Mechanism of Action: It works by dilating blood vessels, particularly veins, leading to decreased cardiac preload and oxygen demand, thus improving myocardial oxygen supply-demand balance.

• Dosage Strength: Each 10 mL ampoule contains 25 mg of Nitroglycerin, providing a standardized dose for intravenous administration.

• Onset of Action: Rapid onset of action allows for quick symptom relief, making it suitable for acute situations where immediate intervention is required.

• Medical Supervision: Administration should be under the close supervision of healthcare professionals due to the potential for significant hemodynamic effects, including hypotension.

• Side Effects: Common side effects may include headache, dizziness, and flushing. Hypotension may occur, particularly with rapid infusion.

• Contraindications: Avoid in patients with severe hypotension or increased intracranial pressure due to the risk of worsening these conditions.

• 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.

Nitroglycerin Injection 25 MG/10 ML provides rapid symptom relief and hemodynamic stabilization in acute episodes of angina and congestive heart failure, making it a valuable medication in emergency cardiovascular care.

Additional Information:

• Packaging Details: 5 AMPOULES PER BOX

Strength	5000 IU
Packaging Type	10 VIALS PER BOX
Packaging Size	5 ml
Brand	CAPRIN
Usage	Treatment and prevention of blood clots
Manufacturer Name	SAMARTH LIFESCIENCES
Prescription/ Non Prescription	Prescription

Product Name: Heparin Sodium Injection
Brand Name: Caprin
Strength: 5,0000 IU/5 ML
Packing: 10 Vial Per Box

Description:

Caprin (Heparin Sodium Injection 5,000 IU/5 mL) is a sterile, preservative-free anticoagulant solution used to prevent and treat blood clots. It is a fast-acting anticoagulant that works by inhibiting thrombin and activated Factor Xa through potentiation of antithrombin III, thereby suppressing the formation and growth of thrombi. It is widely used in hospitals to manage thromboembolic disorders and in procedures requiring anticoagulation, such as dialysis and surgeries.

Composition (per 5 mL):

• Heparin Sodium IP: 5,000 IU

• Water for Injection: q.s.

Indications:

• Prophylaxis and treatment of venous thrombosis and pulmonary embolism

• Prevention of clotting in arterial and cardiac surgery

• Anticoagulation during hemodialysis

• Prevention of deep vein thrombosis (DVT) in at-risk patients

• Disseminated intravascular coagulation (DIC)

• Maintenance of catheter patency

Strength	1500000 IU
Dose/Strength	15 Lac i.u/vial
Brand	Streptokinase
Indication	PE
Route of Administration	IV infusion
Usage	Emergency, Hospital, ICU, Cath lab
Packaging Type	Vial
form	injection
pack size	1 vial
composition	Streptokinase for Injection 15000 IU
brand name	Stukinase

Product Name: Streptokinase For Injection
Brand Name: Stukinase
Strength: 15000 IU
Packing: Single Vial Per Box

Streptokinase For Injection is a thrombolytic medication primarily used to dissolve blood clots in conditions such as myocardial infarction (heart attack), pulmonary embolism, and deep vein thrombosis. Here's a concise overview with pointers:

• Medical Use: Administered to break down blood clots (thrombi) that have formed within blood vessels, restoring blood flow and preventing tissue damage.

• Mechanism of Action: Acts as an enzyme that converts plasminogen to plasmin, which then degrades fibrin, the main component of blood clots.

• Dosage Form: Provided as a lyophilized powder for reconstitution into a solution for intravenous administration, ensuring rapid delivery to the bloodstream.

• Onset of Action: Rapid onset of action allows for quick dissolution of blood clots, reducing the risk of complications associated with thrombosis.

• Medical Supervision: Administration should be performed under the supervision of healthcare professionals experienced in thrombolytic therapy, as it carries the risk of bleeding complications and allergic reactions.

• Side Effects: Common side effects may include bleeding, allergic reactions, and fever. Serious adverse reactions such as intracranial hemorrhage may occur, requiring immediate medical attention.

• Contraindications: Avoid in patients with active bleeding, recent surgery or trauma, or a history of stroke, intracranial hemorrhage, or severe uncontrolled hypertension.

• 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.

Streptokinase For Injection is a crucial medication in the management of thrombotic conditions, offering rapid and effective dissolution of blood clots to restore blood flow and prevent further complications.

Additional Information:

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

Packaging Type	Vial
Brand	SUXIM
Treatment	Muscle Relaxation for Intubation
Packaging Size	10 x 2ml
Shelf Life	18 months
Manufacturer	Samarth Lifesciences
Country of Origin	Made in India
Strength	100 MG / 2 ML
Packing type	10 AMPOULES PER BOX

Strength	50mg/1ml
Pack Size	1 ml
Pack Type	Ampoule
Route	IV
Brand	FENOXENE
Prescription	Prescription
Form	Injection
Shelf Life	18 months

Product Name: Phenoxybenzamine Injection
Brand Name: Fenoxene
Strength: 50MG/1ML
Packing: Single Ampoules Per Box

Packaging Type	Vial
Brand	Nipress
Treatment/Indication	Cardiac Surgery
Packaging Size	5 ml
Strength	50 mg/2 mL
Manufacturer	Samarth life science Pvt. ltd
Form	Injection
Country of Origin	Made in India

Product Name: Sodium Nitroprusside for Injection 50 MG
Brand Name: Nipress
Strength: 50 MG
Packing: Single vial per box

• Drug Name: Sodium Nitroprusside for Injection
• Purpose: Used for the rapid reduction of blood pressure in hypertensive emergencies or perioperative hypertension.
• Mechanism of Action: Acts as a potent vasodilator by releasing nitric oxide, leading to relaxation of smooth muscle in blood vessels, thus reducing blood pressure.
• Formulation: Available as a sterile, clear, colorless solution for intravenous administration.
• Dosage: Administered by a healthcare professional as an intravenous infusion, with dosage adjusted based on blood pressure response and patient's clinical condition.
• Onset of Action: Rapid onset of action, with effects typically seen within minutes after administration.
• Adverse Effects: Possible side effects include excessive hypotension, cyanide toxicity (especially with prolonged use or high doses), metabolic acidosis, tachycardia, and nausea.
• Precautions: Close monitoring of blood pressure, heart rate, and signs of cyanide toxicity is essential during treatment. Use caution in patients with impaired renal or hepatic function.
• Contraindications: Contraindicated in patients with known hypersensitivity to sodium nitroprusside or other nitrovasodilators.
• Storage: Store the solution at controlled room temperature, protected from light. Discard any unused portion of the solution as per healthcare facility protocols.
• Availability: Typically prescribed in hospital settings or emergency departments, administered by healthcare professionals experienced in managing hypertensive emergencies.
• Follow-Up: Continuous monitoring of blood pressure and clinical status is necessary during treatment. Adjustments to the infusion rate may be required based on the patient's response.

Additional Information:

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

Grade Standard	Bio-Tech Grade
Purity	85%
Form	Liquid
Type	Mono Potassium Phosphate
Packaging Size	12 ML
Application	Pharmaceutical
Usage/Application	Pharmaceutical Industry
Country of Origin	Made in India
Brand Name	Potphate
Packing	Single Vial Per Box

Product Name: Postassium Phosphates Injection
Brand Name: Potphate
Strength: 15 ML
Packing: Single Vial Per Box

Description:
Potassium Phosphates Injection is a sterile, non-pyrogenic solution of a mixture of monobasic and dibasic potassium phosphate. It is used to replenish phosphorus and potassium in patients with significant deficiencies due to various clinical conditions such as diabetic ketoacidosis, hyperalimentation, or prolonged vomiting.

Indications:
Treatment and prevention of hypophosphatemia
Correction of concurrent hypokalemia
Phosphate supplementation in TPN (Total Parenteral Nutrition)

Key Benefits:
Dual supplementation of potassium and phosphate
Sterile, ready-to-use formulation
Trusted for critical care and nutritional support

Packaging:
Available in multiple volumes and concentrations to suit varied clinical needs.

Additional Information:

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

Concentration	15% w/v
Form	Liquid
Pack Size	10 ml
Diluent Base	KCl in dextrose
Packaging Size	10 ml
Route of Administration	IV infusion
Pack Type	Ampoule
Usage	Hospital
Packaging Type	Bottle
Country of Origin	Made in India
Brand	POTLYTE
Purity	90%
Packing	5 Ampoules Per Box

Product Name: Potassium Chloride Concentrate Injection
Brand Name: Potltye
Stength: 1.5 GM/ 10 ML
Packing: 5 Ampoules Per Box

1. Medication Name: Potassium Chloride Concentrate Injection
2. Type: Injectable solution
3. Purpose: Used to treat or prevent low levels of potassium in the blood (hypokalemia).
4. Dosage Strength:
   • Available in various concentrations, typically ranging from 1 to 2 mEq/mL.
5. Administration:
   • Administered intravenously by a healthcare professional.
6. Mechanism of Action:
   • Potassium chloride supplements the body's potassium levels, essential for normal cell function, muscle contraction, and nerve transmission.
7. Indications:
   • Treatment and prevention of hypokalemia associated with conditions such as diuretic therapy, gastrointestinal losses, or metabolic disorders.
8. Contraindications:
   • Hypersensitivity to potassium chloride or any component of the formulation.
   • Hyperkalemia (high potassium levels) or conditions predisposing to hyperkalemia, such as severe renal impairment or adrenal insufficiency.
9. Side Effects:
   • Common side effects may include pain at the injection site, phlebitis, and discomfort.
   • Serious side effects may include hyperkalemia, cardiac arrhythmias, and tissue necrosis if extravasation occurs.
10. Precautions:
    • Administration should be slow and diluted to minimize the risk of adverse reactions, especially in patients with cardiac or renal impairment.
    • Regular monitoring of potassium levels, renal function, and electrocardiogram (ECG) is essential during treatment.
11. Storage:
    • Store at room temperature away from light and moisture.
12. Availability:
    • Available by prescription only and typically administered in hospital or clinical settings.
13. Monitoring:
    • Close monitoring of potassium levels, renal function, and cardiac status is necessary during and after administration to prevent potential complications.

Additional Information:

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

Pack Size	10x1ml ampoule
Packaging Size	1ml
Packaging Type	Ampoules
Prescription	Prescription
Brand	CPROSTIN
Strength	250 MCG/ 1 ML
Packing	10 Ampoules per box
Route	IV
Injection Administeration Type	IM

Product Name: Carboprost Tromethamine Injection Ip
Brand Name: Cprostin
Strength: 250 MCG/ 1 ML
Packing: 10 Ampoules per box

Carboprost tromethamine injection IP is a medication primarily used to induce uterine contractions and control postpartum hemorrhage. Here's a brief description with pointers:

1. Purpose: Induces uterine contractions to manage postpartum hemorrhage (excessive bleeding after childbirth) or to induce abortion in cases of fetal demise or medical termination of pregnancy.

2. Administration: Administered intramuscularly by healthcare professionals, typically in a hospital or obstetric setting.

3. Mechanism of Action: Carboprost tromethamine is a prostaglandin analog that stimulates uterine smooth muscle contraction, leading to hemostasis and uterine involution.

4. Indications: Used for the prevention or treatment of postpartum hemorrhage following childbirth or as part of abortion procedures.

5. Dosage: Dosage varies based on the clinical indication, typically administered as a single injection or in divided doses.

6. Onset and Duration: Rapid onset of action within minutes, with effects lasting for several hours.

7. Side Effects: Common side effects may include uterine cramping, nausea, vomiting, diarrhea, fever, and headache. Risk of severe allergic reactions or uterine rupture exists.

8. Contraindications: Avoid use in patients with hypersensitivity to prostaglandins, acute pelvic inflammatory disease, or active cardiac, pulmonary, renal, or hepatic disease.

9. Precautions: Carboprost tromethamine should be used cautiously in patients with asthma, glaucoma, or a history of cesarean section due to the risk of uterine rupture.

10. Storage: Store carboprost tromethamine injection according to manufacturer instructions, typically at controlled room temperature and protected from light.

11. Patient Monitoring: Close monitoring of uterine contractions, vital signs, and any signs of adverse reactions is necessary during and after administration.

12. Follow-Up: Patients receiving carboprost tromethamine should undergo follow-up evaluations to assess the effectiveness of treatment and monitor for complications.

Additional Information:

• Packaging Details: 10 AMPOULES PER BOX