Cefazoline Sodium Injection 1000mg

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MOQ : 5000 Packs, ,

Cefazoline Sodium Injection 1000mg Specification

Dosage
1000mg

Molecular Formula
C14H13N8NaO4S3

Usage
Antibacterial, used to treat a wide variety of bacterial infections

Storage
Store below 25C, protected from light

Expiration Date
24 months from manufacturing date

CAS No
27164-46-1

Salt Composition
Cefazoline Sodium

Pacakaging (Quantity Per Box)
1 vial per box

Medicine Type
Injection

Dosage Form
Powder for injection

Assay
98% (on anhydrous basis)

Appearance
White to off-white crystalline powder

Grade
Pharmaceutical Grade

Origin of Medicine
India

Indication
Treatment of bacterial infections including respiratory tract, skin, urinary tract, and bone/joint infections

Cefazoline Sodium Injection 1000mg Trade Information

Minimum Order Quantity
5000 Packs, ,

FOB Port
Mumbai

Payment Terms
Cash in Advance (CID), Cash Advance (CA)

Supply Ability
100000 Packs, , UNITS Per Month

Delivery Time
45 to 60 days Days

Sample Available
Yes

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
AS PER BUYERS REQUIREMENT.

Main Export Market(s)
Eastern Europe, Australia, Western Europe, North America, South America, Middle East, Africa, Central America, Asia

Main Domestic Market
All India

Certifications
WHO GMP,ISO,FSSAI

About Cefazoline Sodium Injection 1000mg

Experience the radiant effectiveness of Cefazoline Sodium Injection 1000mgyour superlative choice for combating serious bacterial infections. Prepared as a fresh, sterile powder, this laureate pharmaceutical grade formulation is soluble in water and designed for intravenous or intramuscular administration. Each select glass vial offers 98% assay purity, ensuring confidence in quality and potency. Manufactured in ISO 9001 and WHO-GMP certified facilities in India, this antibiotic must be reconstituted with sterile water before use. Grab yours today, protected by a robust shelf life of 2 years.

Cefazoline Sodium Injection 1000mg: Features, Usage, and Applications

This injection is a select, pharmaceutical-grade antibacterial agent, supplied as a white, crystalline powder. Used by healthcare professionals, it treats a spectrum of infectionsrespiratory, urinary, skin, bone, and joints. With its reconstitution flexibility (intravenous or intramuscular), precise dosage, and ISO-certified sterility, its a preferred choice for both hospitals and clinics. Its fresh, radiant formulation ensures superlative results in infection control, trusted by doctors and pharmacists alike.

Main Export Markets, Express Sample Outlay, and Supply Capacity

Distributed worldwide from India, Cefazoline Sodium Injection 1000mg boasts robust outlay across Asia, Africa, the Middle East, and Eastern Europe. Express shipping is available for urgent orders, and samples are provided upon quotation. With high supply ability for bulk purchasing and prompt fulfillment, global dealers, exporters, and wholesalers can rely on consistent quality and timely delivery, positioning this product as a staple in international pharmaceutical trade.

FAQs of Cefazoline Sodium Injection 1000mg:

Q: How is Cefazoline Sodium Injection 1000mg administered?

A: Cefazoline Sodium Injection 1000mg should be reconstituted with sterile water and administered either intravenously (IV) or intramuscularly (IM), as directed by a healthcare professional.

Q: What conditions can Cefazoline Sodium Injection treat?

A: Cefazoline Sodium Injection is used to treat a wide variety of bacterial infections, including those of the respiratory tract, urinary tract, skin, bones, and joints.

Q: When should this injection be used?

A: This injection should be used upon a doctors prescription, typically when bacterial infections are suspected or confirmed and suitable based on the infections severity and location.

Q: Where is Cefazoline Sodium Injection manufactured and exported from?

A: Cefazoline Sodium Injection is manufactured and exported from India, produced in ISO 9001 and WHO-GMP certified facilities ensuring pharmaceutical-grade excellence.

Q: What is the process for reconstituting this injection?

A: The process involves adding a specified amount of sterile water for injection directly into the glass vial, agitating gently until the powder is fully dissolved before administration.

Q: What are the benefits of using this pharmaceutical grade sterile powder?

A: The benefits include precise antibacterial efficacy, high assay purity (98%), and a stable shelf life, making it suitable for a broad range of acute bacterial infections.

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