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IMIPENEM CILASTATIN INJECTION
IMIPENEM CILASTATIN INJECTION

IMIPENEM CILASTATIN INJECTION

MOQ : 5000 Packs

IMIPENEM CILASTATIN INJECTION Specification

  • Salt Composition
  • Imipenem 500 mg + Cilastatin 500 mg
  • Indication
  • Serious bacterial infections (respiratory tract, urinary tract, intra-abdominal, gynecological, skin and soft tissue, bone and joint, septicemia, endocarditis)
  • Dosage Form
  • Injection
  • Enzyme Types
  • Other
  • Feature
  • Other
  • Ingredients
  • Other
  • Application
  • Other
  • Ph Level
  • 6.5 to 7.5 (approximate, reconstituted solution)
  • Physical Color/Texture
  • White to off-white lyophilized powder
  • Fermentation Smell
  • Normal Smell
  • Storage Instructions
  • NORMAL TEMP
  • Shelf Life
  • 2 Years
 

IMIPENEM CILASTATIN INJECTION Trade Information

  • Minimum Order Quantity
  • 5000 Packs
  • FOB Port
  • Mumbai
  • Payment Terms
  • Cash in Advance (CID), Cash Advance (CA)
  • Supply Ability
  • Pack
  • Delivery Time
  • Days
  • Sample Available
  • Yes
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • STANDARD PACKING
  • Certifications
  • WHO GMP,ISO,FSSAI
 

About IMIPENEM CILASTATIN INJECTION



Unlock the full therapeutic potential of IMIPENEM CILASTATIN INJECTION, a harmonious blend formulated for inestimable efficacy against serious bacterial infections. Highlighted by its remarkable ability to address respiratory, urinary, intra-abdominal, and other critical infections, this wondrous formulation is designed for intravenous use in hospitals and clinical settings. Procure this Schedule H, sterile, single-use vial to ensure the highest standard of care. Its compatibility with 0.9% sodium chloride offers seamless administration, and the products stability and potency guarantee exceptional outcomes for patients in need.

Application and Clinical Uses

IMIPENEM CILASTATIN INJECTION finds its primary application within hospital environments, supporting the treatment of serious bacterial infections. This sterile white to off-white lyophilized powder is intended for use on human patients via intravenous (IV) administration. Its use type is strictly prescription-based, underscoring its suitability for clinical surfaces and healthcare professionals. The formulation is ideal for combating infections of the respiratory tract, urinary tract, intra-abdominal region, and other major systems, ensuring broad coverage where it matters most.


Packaging, Certifications, and Delivery

Each IMIPENEM CILASTATIN INJECTION is meticulously packed in a glass vial with a flip-off cap, supporting product sterility. Certified for pharmaceutical quality and safety, the packaging guarantees protection throughout the supply chain. Order completion and order processing are designed for efficiency, with delivery time tailored to meet urgent clinical demands. Take advantage of competitive sale prices and streamlined procurement for hospitals, ensuring a prompt and reliable supply when it is needed in critical care scenarios.


FAQs of IMIPENEM CILASTATIN INJECTION:


Q: How is IMIPENEM CILASTATIN INJECTION administered?

A: IMIPENEM CILASTATIN INJECTION is administered intravenously after reconstitution with a suitable diluent, typically 0.9% sodium chloride, under medical supervision in a hospital or healthcare facility.

Q: What are the highlighted indications for this injection?

A: This injection is indicated for serious bacterial infections, including those affecting the respiratory tract, urinary tract, intra-abdominal area, gynecological sites, skin and soft tissue, bones and joints, septicemia, and endocarditis.

Q: When should IMIPENEM CILASTATIN INJECTION not be used?

A: IMIPENEM CILASTATIN INJECTION should not be used in patients with known hypersensitivity to beta-lactams or in those with contraindicated conditions, as advised by medical professionals.

Q: Where should the reconstituted solution be stored, and for how long?

A: The reconstituted solution should be used promptly or stored as per healthcare guidance, usually at normal room temperature, ensuring utilization within the recommended timeframe to maintain potency and sterility.

Q: What is the process for order completion and delivery?

A: Order processing begins upon confirmation, and the vials are packed securely. Order completion and dispatch are expedited to fulfill urgent clinical demands, and sale price options are available for bulk procurement.

Q: How does the procurement benefit hospitals and clinics?

A: Procuring this injection supports uninterrupted patient care by providing a sterile, reliable, and high-quality treatment option for life-threatening infections, endorsed with appropriate certifications and a practical pack size.

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