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Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection
Third Party Manufacturing for Dobutamine 50mg Injection

Third Party Manufacturing for Dobutamine 50mg Injection

Price 999.0 INR/ Vial

MOQ : 100 Boxes

Third Party Manufacturing for Dobutamine 50mg Injection Specification

  • Lead Time
  • 4-6 weeks after order confirmation
  • Feature
  • Sterile, ready-to-use, accurate dosing, complies with GMP standards
  • Precautions
  • To be used under medical supervision only; monitor cardiac parameters during administration
  • Life Span
  • 24 months
  • Weight
  • Standard as per packaging
  • Appearance
  • Clear, colorless to slightly yellow liquid
  • Composition
  • Each ml contains Dobutamine Hydrochloride 50mg
  • Color
  • Colorless to faint yellow
  • Product Type
  • Pharmaceutical Injectable
  • Ingredients
  • Other
  • Physical Form
  • Liquid Injection
  • Treatments & Functions
  • Cardiac stimulant, Used to treat heart failure and cardiogenic shock
  • Recommended For
  • Other Health Issues
  • Age Group
  • Adults, Elderly
  • Dosage Guidelines
  • Other
  • Quantity
  • Ampoule or vial; available in standard 5ml and 10ml formats
  • Packaging
  • Other
  • Storage Instructions
  • Store below 25C, protect from light and moisture
  • Marketed By
  • Offered under third party/contract manufacturing agreements
  • Shelf Life After Opening
  • Use immediately after opening
  • Diluent Compatibility
  • Compatible with 5% Dextrose and 0.9% Sodium Chloride Injection
  • Manufacturing Capacity
  • 100,000 units per month
  • Injection Route
  • Intravenous infusion or injection
  • Regulatory Approvals
  • Compliant with Indian Pharmacopoeia/US FDA guidelines (as per client requirement)
 

Third Party Manufacturing for Dobutamine 50mg Injection Trade Information

  • Minimum Order Quantity
  • 100 Boxes
  • Supply Ability
  • 1000 Boxes Per Month
  • Delivery Time
  • 7 Days
 

About Third Party Manufacturing for Dobutamine 50mg Injection

Monark Biocare is the trusted ISO certified Pharma Company in Mysuru. With a decade of experience, we have cemented our position as trusted manufacturers and suppliers of top-notch pharmaceutical products across India. We are WHO-GMP, GLP certified company in India with the exclusive range of pharma products. Our extensive product portfolio includes a diverse range of tablets, capsules, injectables, syrups, ointments, nasal drops, etc.

Sterile and Accurate Dosing

Every batch of Dobutamine 50mg Injection is produced under stringent GMP standards to ensure sterility and precise dosing. Compliance with key regulatory standards guarantees consistent quality and safety for critical care applications. The product is provided in glass ampoules or vials, supporting safe and efficient intravenous infusion in clinical settings.


Versatility in Cardiac Care

This injection is widely used in cardiac care centers and hospitals to manage acute heart failure and cardiogenic shock. Its compatibility with standard diluents (5% Dextrose or 0.9% Sodium Chloride) simplifies integration into existing treatment protocols. Quick lead times and flexible packaging options allow for efficient supply chain management tailored to institutional needs.

FAQ's of Third Party Manufacturing for Dobutamine 50mg Injection:


Q: How is Dobutamine 50mg Injection administered?

A: Dobutamine 50mg Injection is intended for intravenous infusion or injection, typically under the direct supervision of a healthcare professional. The dosage and rate of administration are determined by a physician based on the patient's clinical condition.

Q: What diluents are compatible with Dobutamine 50mg Injection?

A: This injection is compatible with 5% Dextrose and 0.9% Sodium Chloride Injection, making it convenient for routine hospital and clinical use.

Q: When should Dobutamine 50mg Injection be used after opening?

A: The injection should be used immediately after opening the ampoule or vial to maintain sterility and product efficacy. Any remaining solution should be discarded.

Q: Where is Dobutamine 50mg Injection manufactured and supplied?

A: Dobutamine 50mg Injection is offered under third party/contract manufacturing agreements in India, with full compliance to Indian Pharmacopoeia or US FDA guidelines as per client requirements. It is distributed to hospitals, clinics, and cardiac care centers across the country.

Q: What is the manufacturing capacity and lead time for this injection?

A: Our manufacturing facility can produce up to 100,000 units of Dobutamine 50mg Injection per month. The standard lead time from order confirmation is 4-6 weeks, ensuring stable and timely supply.

Q: What are the key benefits of third party manufacturing for Dobutamine 50mg Injection?

A: Third party manufacturing ensures consistent product quality, regulatory compliance, and reliable supply. It allows healthcare providers to access high-quality cardiac care products without investing in their own production infrastructure.

Q: Are there any storage and usage precautions for this product?

A: Yes, the injection should be stored below 25C, away from light and moisture, and used only under medical supervision. Cardiac parameters should be monitored during administration, and the product is intended for adults and elderly patients only.

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