Service Location	PAN India
Certification	ISO, WHO, GMP
Pharmaceutical Experience	Above 10 Years
Delivery Time	Immediate
Territory Rights	Monopoly Right
Form Of Medicine	INJECTION, Capsule
Promotional Material	Visiting Cards, Visual Aids, Brochure
Number Of Already Existing Franchises	100+
Number Of Products Offered	500+

 

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

 

Additional Information:

• Item Code: P0707
• Production Capacity: 5000000
• Delivery Time: IMMEDIATE
• Packaging Details: AS PER NORMS AND SPECIFICATION

Service Mode	Offline
Service Duration	24 Months
Certification	GMP, GLP, ISO, WHO
Pharmaceutical Experience	Above 10 Years
Delivery Time	Within a Month
Form of Medicine	Injection
Type of Injection	Intravenous, Subcutaneous, Intramuscular, Lyophilized
Production Capacity	Large Scale, Small Scale, Medium Scale
Number Of Existing Clients	100
Promotional Material	Calendars, Notepads, Visiting Cards, Writing Pads, Pens, Working Bag, Diaries, Visual Aids, Bottle
Product List Available	Yes
Range of Products	Antacids, Orthopedic, Gynaecology, Gastrointestinal, Neurological, Antihistamines, Cardiac Diabetic, Pediatrics, Antibiotics, Antimicrobials, Ophthalmic, Anti Cancer, Derma
Medicine Type	Allopathic
Payment	Online

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: T01
• Production Capacity: 50000000
• Delivery Time: 40 to 60 Days
• Packaging Details: As per Requirements.

Strength	500 mg
Pack Size	20 ml
Pack Type	Box
Manufacturer	Wizard Venture
Prescription/Non Prescription	Prescription
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Country of Origin	Made in India

Meropenem is a broad-spectrum antibiotic that belongs to the carbapenem class. It is used to treat a variety of bacterial infections. Here are some key points about Meropenem:

 

Type: Antibiotic (carbapenem)

 

Mechanism of Action:

 

Meropenem exerts its bactericidal (kills bacteria) effect by interfering with the synthesis of bacterial cell walls. It is effective against a wide range of bacteria.

Indications:

 

Meropenem is used to treat serious infections caused by susceptible bacteria.

Common indications include complicated intra-abdominal infections, complicated skin and soft tissue infections, bacterial meningitis, and nosocomial pneumonia.

Administration:

 

Meropenem is typically administered intravenously (IV) by a healthcare professional.

The dosage and duration of treatment depend on the type and severity of the infection, as well as the patient's individual factors.

Common Side Effects:

 

Like any antibiotic, meropenem may cause side effects. Common side effects include diarrhea, nausea, headache, and rash.

Serious side effects are rare but can include allergic reactions, seizures, and inflammation of the colon.

Monitoring:

 

Patients receiving meropenem may require regular monitoring, especially if they have pre-existing conditions or are taking other medications.

Precautions:

 

It's important to inform the healthcare provider about any allergies, medical conditions, or medications being taken before starting meropenem.

The drug is usually reserved for serious infections and is not typically used for mild or routine infections.

Dosage:

 

The dosage is determined by the healthcare provider based on factors such as the type of infection, the patient's weight, and renal function.

It's crucial for patients to complete the entire prescribed course of meropenem, even if symptoms improve before the medication is finished. Incomplete treatment may lead to the development of antibiotic-resistant bacteria.

 

As with any medication, patients should consult with their healthcare provider for personalized advice and to discuss potential risks and benefits, especially considering individual health conditions and medical history.

Additional Information:

• Item Code: INJ07
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise and 40 to 60 days in own Brand

Strength	250 mg
Pack Size	10 ml
Brand Name	Wipen
Pack Type	Box
Injection Site	IV only
Manufacturer	Wizard Venture
Prescription/Non Prescription	Prescription
Composition	Meropenem
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Country of Origin	Made in India

Meropenem is a broad-spectrum antibiotic that belongs to the carbapenem class. It is used to treat a variety of bacterial infections. Here are some key points about Meropenem:

 

Type: Antibiotic (carbapenem)

 

Mechanism of Action:

 

Meropenem exerts its bactericidal (kills bacteria) effect by interfering with the synthesis of bacterial cell walls. It is effective against a wide range of bacteria.

Indications:

 

Meropenem is used to treat serious infections caused by susceptible bacteria.

Common indications include complicated intra-abdominal infections, complicated skin and soft tissue infections, bacterial meningitis, and nosocomial pneumonia.

Administration:

 

Meropenem is typically administered intravenously (IV) by a healthcare professional.

The dosage and duration of treatment depend on the type and severity of the infection, as well as the patient's individual factors.

Common Side Effects:

 

Like any antibiotic, meropenem may cause side effects. Common side effects include diarrhea, nausea, headache, and rash.

Serious side effects are rare but can include allergic reactions, seizures, and inflammation of the colon.

Monitoring:

 

Patients receiving meropenem may require regular monitoring, especially if they have pre-existing conditions or are taking other medications.

Precautions:

 

It's important to inform the healthcare provider about any allergies, medical conditions, or medications being taken before starting meropenem.

The drug is usually reserved for serious infections and is not typically used for mild or routine infections.

Dosage:

 

The dosage is determined by the healthcare provider based on factors such as the type of infection, the patient's weight, and renal function.

It's crucial for patients to complete the entire prescribed course of meropenem, even if symptoms improve before the medication is finished. Incomplete treatment may lead to the development of antibiotic-resistant bacteria.

 

As with any medication, patients should consult with their healthcare provider for personalized advice and to discuss potential risks and benefits, especially considering individual health conditions and medical history.

Additional Information:

• Item Code: INJ012
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise and 40 to 60 days in Third Party Manufacturing
• Packaging Details: Vial with SWFI

Strength	1 gm
Pack Size	20 ml
Pack Type	Vial
Certification	ISO, GLP, WHO
Form of Medicine	Injection
Prescription/Non Prescription	Prescription
Promotional Material	Diaries, Notepads, Visual Aids, Pens, Brochure, Writing Pads
Range of Products	Antibiotics, Antimicrobials
Shelf Life	24 months
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Country of Origin	Made in India

Meropenem is a broad-spectrum antibiotic that belongs to the carbapenem class. It is used to treat a variety of bacterial infections. Here are some key points about Meropenem:

 

Type: Antibiotic (carbapenem)

 

Mechanism of Action:

 

Meropenem exerts its bactericidal (kills bacteria) effect by interfering with the synthesis of bacterial cell walls. It is effective against a wide range of bacteria.

Indications:

 

Meropenem is used to treat serious infections caused by susceptible bacteria.

Common indications include complicated intra-abdominal infections, complicated skin and soft tissue infections, bacterial meningitis, and nosocomial pneumonia.

Administration:

 

Meropenem is typically administered intravenously (IV) by a healthcare professional.

The dosage and duration of treatment depend on the type and severity of the infection, as well as the patient's individual factors.

Common Side Effects:

 

Like any antibiotic, meropenem may cause side effects. Common side effects include diarrhea, nausea, headache, and rash.

Serious side effects are rare but can include allergic reactions, seizures, and inflammation of the colon.

Monitoring:

 

Patients receiving meropenem may require regular monitoring, especially if they have pre-existing conditions or are taking other medications.

Precautions:

 

It's important to inform the healthcare provider about any allergies, medical conditions, or medications being taken before starting meropenem.

The drug is usually reserved for serious infections and is not typically used for mild or routine infections.

Dosage:

 

The dosage is determined by the healthcare provider based on factors such as the type of infection, the patient's weight, and renal function.

It's crucial for patients to complete the entire prescribed course of meropenem, even if symptoms improve before the medication is finished. Incomplete treatment may lead to the development of antibiotic-resistant bacteria.

 

As with any medication, patients should consult with their healthcare provider for personalized advice and to discuss potential risks and benefits, especially considering individual health conditions and medical history.

Additional Information:

• Item Code: INJ001
• Production Capacity: 50000
• Delivery Time: Immediate iin PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Available with water, with and without tray pack.

Strength	600 mg
Quantity Unit	Ampoules
Antibiotic	Injection
Pack Size	4 ml
Pack Type	Box
Treatment	Treatment Of Serious Infections, Especially When Other Antibiotics Have Been Unable To Clear The In

Clindamycin is a lincosamide antibiotic that is used to treat bacterial infections in both humans and animals. It is effective against a variety of Gram-positive and anaerobic bacteria. Here are some key points about Clindamycin injection:

 

Type: Antibiotic (lincosamide)

 

Mechanism of Action: Clindamycin inhibits bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome.

Indications:

 

Clindamycin is used to treat bacterial infections in various tissues and organs, including skin and soft tissue infections, dental infections, bone infections, respiratory tract infections, and certain types of bacterial septicemia.

Administration:

 

Clindamycin is available in various forms, including oral capsules, oral liquid, and injectable forms. The injectable form is administered intravenously (IV) or intramuscularly (IM) by a healthcare professional.

Dosage:

 

The dosage of Clindamycin depends on the type and severity of the infection, the patient's weight, and individual factors. It is determined by a healthcare provider.

Applications:

 

Skin and Soft Tissue Infections: Clindamycin is often used to treat skin and soft tissue infections caused by susceptible bacteria.

Bone Infections: It may be prescribed for bone infections, including osteomyelitis.

Respiratory Infections: Clindamycin is sometimes used for respiratory tract infections caused by susceptible organisms.

Side Effects:

 

Common side effects may include gastrointestinal symptoms such as nausea, vomiting, or diarrhea. More serious side effects are rare but can include severe colitis (inflammation of the colon).

Precautions:

 

Clindamycin should be used with caution in individuals with a history of gastrointestinal disease, especially colitis.

It's important to inform the healthcare provider about any allergies, medical conditions, or medications being taken before starting Clindamycin.

Monitoring:

 

Monitoring for potential side effects and efficacy is typically done during the course of treatment.

It's crucial to complete the full course of treatment as prescribed by the healthcare provider, even if symptoms improve before the medication is finished. As with any antibiotic, misuse or overuse can contribute to antibiotic resistance. If you have questions or concerns about Clindamycin or its use, it's recommended to consult with a healthcare professional.

Additional Information:

• Item Code: NIJ01
• Production Capacity: 500000
• Delivery Time: Immediate in PCD & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 4*5 ml Tray PAck

Strength	500 mg
Packaging Type	Box
Composition	500 mg Of Acyclovir And 49 mg Of Sodium
Brand	Zaravir- Zara
Manufacturer	Zara
Treatment	Treating Viral Infections Like Herpes Labialis, Herpes Simplex Virus Infections, Shingles, Genital
Prescription/Non prescription	Prescription
Form	Injection
Also gives	PCD Pharma, Third Party Manufacturing
Country of Origin	Made in India

Acyclovir is an antiviral medication commonly used for the treatment of infections caused by the herpes simplex virus (HSV) and the varicella-zoster virus (VZV). It is available in various forms, including oral tablets, topical creams, and intravenous (IV) injections.

 

Acyclovir injection is typically administered in a healthcare setting, such as a hospital, clinic, or infusion center, under the supervision of healthcare professionals. The IV form of acyclovir is often used for severe cases of HSV or VZV infections, particularly in immunocompromised individuals or those with severe complications.

 

Here are some key points about acyclovir injection:

 

Indications: Acyclovir injection is commonly used for the treatment of severe cases of herpes simplex infections, such as encephalitis (inflammation of the brain) caused by HSV, and for severe cases of varicella-zoster infections, including herpes zoster (shingles) in immunocompromised patients.

 

Administration: Acyclovir injection is administered by healthcare professionals through an intravenous (IV) line. The dosage and duration of treatment depend on the specific condition being treated, the severity of the infection, and the patient's overall health.

 

Monitoring: Patients receiving acyclovir injection are typically monitored closely for any adverse reactions or side effects. Common side effects may include nausea, vomiting, diarrhea, and headache. In rare cases, more serious side effects, such as kidney problems, may occur.

 

Precautions: It is important to inform healthcare providers about any pre-existing medical conditions, allergies, or medications the patient is taking before starting acyclovir treatment. This includes providing information about kidney function, as acyclovir is primarily excreted through the kidneys.

 

Pregnancy and Lactation: Pregnant or breastfeeding individuals should discuss the potential risks and benefits of acyclovir treatment with their healthcare providers. Acyclovir does pass into breast milk, and caution is advised.

 

Resistance: Prolonged or inappropriate use of acyclovir can contribute to the development of drug-resistant strains of the herpes virus. Therefore, it is essential to use acyclovir under the guidance of a healthcare professional and according to prescribed instructions.

 

It's important to note that the information provided here is for general informational purposes. If acyclovir injection is recommended, it should be administered by healthcare professionals, and the specific dosage and treatment plan should be determined by a qualified healthcare provider based on the individual patient's condition.

Additional Information:

• Item Code: INJ040
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: As per Requirements.

Strength	500 mg
Manufacturer	WHO-GMP CERTIFIED
Packaging Type	10 ML
Packaging size	10 ML VIAL WITH MONO CARTON
Country of Origin	Made in India
AVAILABLE FOR	PCD FRANCHISE ON MONOPOLY BASIS
ALSO PROVIDE	THIRD PARTY MANUFACTURING
CERTIFICATION	ISO GMP WHO

FERRIC CARBOXYMALTOSE INJECTION 500 MG

 

Overview:

Ferric Carboxymaltose is an intravenous iron replacement product used to treat iron deficiency anemia (IDA), especially in patients who cannot tolerate or respond inadequately to oral iron therapy.

 

Composition:

Ferric Carboxymaltose equivalent to Elemental Iron 500 mg

 

Dosage Form: Injection

 

Route: Intravenous (IV)

 

Indications:

Iron deficiency anemia in:

 

Chronic kidney disease (non-dialysis and dialysis-dependent)

 

Inflammatory bowel disease

 

Heavy menstrual bleeding

 

Postpartum anemia

 

Intolerance to or failure of oral iron therapy

 

Mechanism of Action:

Ferric Carboxymaltose is a colloidal iron–carbohydrate complex. After IV administration, the iron is released and incorporated into ferritin, the body's iron storage protein, helping restore hemoglobin and replenish iron stores.

 

Dosage:

Adults: Typically 500 mg to 1000 mg per week, not exceeding 1000 mg per dose.

 

Administered as:

 

IV push over at least 15 minutes

 

OR

 

IV infusion diluted in 100–250 mL normal saline over 15–30 minutes

 

Side Effects:

Common: Nausea, headache, dizziness, flushing, hypertension, injection site reactions

 

Serious (rare): Anaphylactic reactions, hypotension, hypophosphatemia

 

Precautions:

Test for iron overload before therapy

 

Monitor serum ferritin and transferrin saturation (TSAT)

 

Use caution in patients with liver disease or active infections

 

Not recommended in first trimester of pregnancy

 

Storage:

Store below 25°C, protect from light

 

Do not freeze

Additional Information:

• Item Code: FCM030
• Production Capacity: 5000000
• Delivery Time: IMMEDIATE
• Packaging Details: 10 ML VIAL

Certification	WHO, GMP, GLP
Pharmaceutical Experience	Above 10 Years
Delivery Time	Within a Month
Form of Medicine	Syrup, INJECTION, Tablet, Capsule
Production Capacity	Medium Scale
Number Of Existing Clients	500+
Also Gives	PCD Pharma Franchise, Third Party Manufacturing

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: JMM03
• Production Capacity: 5000000
• Delivery Time: IMMEDIATE
• Packaging Details: BEST

Injection Site	IV
Composition	Piperacillin Tazobactam 4.5GM Injection
Shelf Life	24 MONTH
Prescription	Prescription
Packing Size	30ML VIAL WITH WATER & TRAY PACK
Service Mode	002
Shelf Life from manufacture	24 MONTH
Packaging Type	Vial
Form	Powder
Country of Origin	Made in India

.

Piperacillin-tazobactam is a combination medication that consists of two active ingredients: piperacillin and tazobactam. Here's an overview of each component:

 

Piperacillin:

 

Type: Antibiotic (extended-spectrum penicillin)

Mechanism of Action: Piperacillin inhibits the synthesis of bacterial cell walls, leading to the death of susceptible bacteria.

Indications: It is effective against a wide range of bacteria and is used to treat various bacterial infections. Common indications include respiratory tract infections, intra-abdominal infections, skin and soft tissue infections, and urinary tract infections.

Tazobactam:

 

Type: Beta-lactamase inhibitor

Mechanism of Action: Tazobactam is combined with piperacillin to enhance its activity by inhibiting the action of beta-lactamases. Beta-lactamases are enzymes produced by some bacteria that can inactivate beta-lactam antibiotics like piperacillin.

Indications: Tazobactam is added to piperacillin to extend its spectrum of activity, especially against beta-lactamase-producing bacteria.

Piperacillin-Tazobactam Injection:

 

Usage: This combination is usually administered intravenously (IV) by a healthcare professional.

Indications: Piperacillin-tazobactam is indicated for the treatment of moderate to severe bacterial infections caused by susceptible organisms.

Common Infections Treated: It is commonly used for infections such as intra-abdominal infections, skin and soft tissue infections, pneumonia, and complicated urinary tract infections.

Important Considerations:

 

Dosage: The dosage is determined by the healthcare provider based on the type and severity of the infection, as well as the patient's weight and renal function.

Monitoring: Patients receiving piperacillin-tazobactam may require regular monitoring, especially if they have pre-existing conditions or are taking other medications.

Precautions: It's important to inform the healthcare provider about any allergies, medical conditions, or medications being taken before starting piperacillin-tazobactam.

Completion of Treatment: Patients should complete the full course of treatment as prescribed by their healthcare provider, even if symptoms improve before the medication is finished.

As with any antibiotic, piperacillin-tazobactam may cause side effects, and patients should seek medical attention if they experience any unusual or severe reactions. It's crucial to follow the healthcare provider's instructions and consult with them for personalized advice.

 

 

 

 

 

Additional Information:

• Item Code: PI202
• Production Capacity: 10000
• Delivery Time: Immediate if Ready Stock Required. 40 to 60 Days if Required in OWN Brand
• Packaging Details: 30ML VIAL WITH WATER & TRAY PACK

Form	Injection
Dose	80 mg
Packaging Size	2 ml
Composition	ANTIBIOTIC AND GENERAL RANGE
Strength	AS DIRECTED BY THE PHYSICIAN
Form Of Medicine	Tablet, INJECTABLES, Capsule, Syrup
Promotional Material	Visual Aids, Brochure, Visiting Cards
Medicine Type	Finished Product
Country of Origin	Made in India
CERTIFICATION	WHO-GMP
AVAILABLE FOR	PCD FRANCHISE WITH MONO POLY RIGHT
ALSO DO	CONTRACT MANUFACTURING OF PHARMACEUTICAL
SERVICE	THIRD PARTY AND PCD
ALSO DEALS IN	EXPORT

• CRITICAL CARE MEDICINE 

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: NI01
• Production Capacity: 500000
• Delivery Time: IMMEDIATE
• Packaging Details: AS PER REQUIREMENTS