Ceftazidime Injection 500 mg

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MOQ : 5000 Packs, ,

Ceftazidime Injection 500 mg Specification

Salt Composition
Ceftazidime Pentahydrate

Medicine Type
Allopathic

Assay
Not less than 98%

CAS No
78439-06-2

Storage
Store below 25C, protected from light

Expiration Date
24 Months from manufacture

Indication
Respiratory tract infections, Urinary tract infections, Skin and soft tissue infections, Septicemia

Molecular Formula
C22H22N6O7S2

Pacakaging (Quantity Per Box)
10 Vials per Box

Grade
Pharmaceutical Grade

Dosage
500 mg

Dosage Form
Injection

Usage
Antibacterial, used for severe bacterial infections

Origin of Medicine
India

Appearance
White to off-white crystalline powder

Ceftazidime Injection 500 mg 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)
Australia, North America, Eastern Europe, Western Europe, Africa, Central America, Middle East, South America, Asia

Main Domestic Market
All India

Certifications
WHO GMP,ISO,FSSAI

About Ceftazidime Injection 500 mg

Jump on instant savings with our renowned Ceftazidime Injection 500 mg, an allopathic, pharmaceutical-grade solution for severe bacterial infections. Famed for its masterful efficacy and compliant with IP/USP/EP standards, this towering treatment offers reliable results with scarce chances of resistance. Supplied in glass vials featuring a flip-off seal, the product retains its potent, micronized powder form for up to two years when stored below 25C. Distributed straight from India by leading manufacturers, each batch guarantees not less than 98% assay and is export-ready with full documentation.

Ceftazidime Injection 500 mg: Enhanced Features & Applications

Designed for critical applications, Ceftazidime Injection 500 mg exhibits famed antibacterial strength, specifically targeting respiratory, urinary tract, and skin infections, as well as septicemia. Its masterful formulation of Ceftazidime Pentahydrate ensures a high assay and broad surface activity, providing consistent efficacy in hospital and clinical settings. With its micronized powder and seamless reconstitution using sterile water, the injection delivers robust results in invasive procedures. Healthcare professionals appreciate its dependable action across diverse medical conditions.

Packaging & Sample Policy: Seamless Goods Transport

We take pride in delivering Ceftazidime Injection 500 mg in secure glass vials, ten per box, supporting safe goods transport under non-refrigerated, dry conditions. Samples of the product are available upon request, supported by a fair exchange approach and registration documents. Our pricing model is structured to ensure you receive the lowest price, making this product highly accessible for dealers, exporters, suppliers, and wholesalers. Comprehensive support and sample policies ensure convenience and satisfaction for our valued partners.

FAQs of Ceftazidime Injection 500 mg:

Q: How should Ceftazidime Injection 500 mg be administered?

A: Ceftazidime Injection 500 mg is administered either intravenously or intramuscularly, as directed by a physician. Please ensure reconstitution with sterile water before use.

Q: What infections can be treated using this injection?

A: This product is indicated for the treatment of severe bacterial infections such as respiratory tract infections, urinary tract infections, skin and soft tissue infections, and septicemia.

Q: When does the product expire and how should it be stored?

A: Ceftazidime Injection 500 mg has a shelf life of 2 years, expiring 24 months from manufacture. Store it below 25C and protect from light for optimal stability.

Q: Where is the product manufactured and exported from?

A: This injection is manufactured and exported from India, adhering strictly to IP/USP/EP pharmacopoeial standards.

Q: What documents and compliance certifications are available for this medication?

A: Registration documents and certificates of analysis are available upon request, confirming compliance with relevant pharmacopoeias and quality standards.

Q: How can samples be obtained for product evaluation?

A: Samples are available upon request for registered dealers, exporters, or wholesalers. Contact our team for sample policy details and assistance with the exchange process.

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