1.5 GM Cefuroxime Sodium Injection IP
1.5 GM Cefuroxime Sodium Injection IP

1.5 GM Cefuroxime Sodium Injection IP

MOQ : 50 Vials

1.5 GM Cefuroxime Sodium Injection IP Specification

  • Origin of Medicine
  • India
  • Salt Composition
  • Cefuroxime Sodium 1.5 g
  • Pacakaging (Quantity Per Box)
  • 1 vial per box
  • Brand Name
  • Your Brand
  • Life Span
  • 24 months from manufacturing date
  • Indication
  • Treatment of susceptible bacterial infections
  • Dosage Form
  • Sterile Powder for Solution
  • Packaging Type
  • Vial with sterile water for injection
  • Drug Type
  • Allopathic
  • Ingredients
  • Cefuroxime Sodium
  • Physical Form
  • Injection
  • Function
  • Antibiotic
  • Recommended For
  • Bacterial Infections
  • Dosage
  • As directed by the physician
  • Dosage Guidelines
  • For IV/IM use only
  • Suitable For
  • Adults and children as prescribed
  • Quantity
  • 1.5 g
  • Storage Instructions
  • Store below 25C, protect from light and moisture
  • Marketing Authorization
  • Obtained as per local regulations
  • Batch Number
  • Available on packaging
  • Reconstitution
  • Sterile water for injection provided
  • MRP
  • As per regulatory pricing
  • Route of Administration
  • Intravenous (IV) or Intramuscular (IM)
  • Prescription Required
  • Yes
 

1.5 GM Cefuroxime Sodium Injection IP Trade Information

  • Minimum Order Quantity
  • 50 Vials
  • Payment Terms
  • Cash in Advance (CID)
  • Supply Ability
  • 1000 Vials Per Month
  • Delivery Time
  • 2-5 Days
  • Main Domestic Market
  • All India
 

About 1.5 GM Cefuroxime Sodium Injection IP



Highly recommended for its valorous efficacy against bacterial infections, Your Brand's 1.5 GM Cefuroxime Sodium Injection IP is the invincible choice for healthcare professionals seeking a powerful antibiotic. Jump on this exclusive offer, designed for intravenous (IV) or intramuscular (IM) administration, with each vial containing 1.5 g of sterile powder and sterile water for reconstitution. Perfect for adults and children as prescribed, this allopathic solution is manufactured in India under stringent regulations, with batch numbers clearly labeled and packaging tailored for optimum safety. Prescription required.

Premium Usage, Advantages & Features

1.5 GM Cefuroxime Sodium Injection IP is ideal for the treatment of susceptible bacterial infections in hospitals and clinics. Its highly potent, broad-spectrum activity ensures quick relief and recovery, making it a perfect solution for a fast-paced medical setting. Valorous against tough pathogens, it is suitable for adults and children under medical supervision. The invincible action, rapid solubility, and supplied sterile water for injection make administration safe and efficient.


Comprehensive Packaging & Global Availability

Estimating high demand, each box contains one vial of sterile powder and one ampoule of sterile water, with batch numbers and expiry dates for full traceability. Our stock is ready for immediate shipping, with sales prices as per regulatory standards. Your Brand supplies across major export markets, ensuring quality and reliability. Sample units are available upon request to allow evaluation before bulk purchase, emphasizing confidence in our product's efficacy and packaging integrity.


FAQ's of 1.5 GM Cefuroxime Sodium Injection IP:


Q: How is 1.5 GM Cefuroxime Sodium Injection IP administered?

A: This product is given intravenously (IV) or intramuscularly (IM) by a healthcare professional, after reconstitution with the sterile water provided in the packaging.

Q: What is the main benefit of using this injection?

A: The primary benefit is its potent, broad-spectrum antibiotic action that effectively targets and treats a variety of susceptible bacterial infections in adults and children.

Q: When should Cefuroxime Sodium Injection be used?

A: It should be used as directed by your physician, typically when a bacterial infection is diagnosed that is susceptible to cefuroxime, and as per the recommended dosage and duration.

Q: What is the process for preparing the injection for administration?

A: Reconstitute the sterile powder using the sterile water provided, following the instructions on the packaging or as advised by a healthcare practitioner, ensuring the solution is fully dissolved before IV or IM use.

Q: Where can I check the batch number and expiration date?

A: The batch number and expiration date are clearly printed on the outer packaging and the vial label to ensure full traceability and product reliability.

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