Ceftazidime Active Pharmaceutical Ingredients
Ceftazidime Active Pharmaceutical Ingredients

Ceftazidime Active Pharmaceutical Ingredients

MOQ : 25 Kilograms

Ceftazidime Active Pharmaceutical Ingredients Specification

  • EINECS No
  • 276-260-6
  • Melting Point
  • Not less than 190C (decomposes)
  • Ph Level
  • 4.5 - 6.5 (solution)
  • Structural Formula
  • [Refer to image or chemical databases for structure]
  • Color
  • White to off-white
  • Molecular Weight
  • 546.6 g/mol
  • HS Code
  • 29419090
  • Loss on Drying
  • Not more than 0.5%
  • Boiling point
  • Not applicable (decomposes)
  • Smell
  • Odorless
  • Shelf Life
  • 3 years from date of manufacture
  • Storage
  • Store below 25C in a dry, dark place
  • Solubility
  • Freely soluble in water, sparingly soluble in methanol, practically insoluble in ethanol and chloroform
  • Poisonous
  • Non-poisonous under recommended usage
  • Particle Size
  • D90 < 10 microns
  • Heavy Metal (%)
  • Not more than 0.001%
  • Molecular Formula
  • C22H22N6O7S2
  • Medicine Name
  • Ceftazidime
  • Chemical Name
  • Ceftazidime
  • CAS No
  • 72558-82-8
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Treatment of bacterial infections
  • Purity(%)
  • >=99% (HPLC)
  • Appearance
  • White to off-white crystalline powder
  • Physical Form
  • Solid
  • Identification (IR/UV/HPLC)
  • Complies with standards
  • Sterility
  • Non-sterile (API form)
  • Residual Solvents
  • Complies with ICH Q3C guidelines
  • By-products/Impurities
  • Complies with pharmacopoeial standards (USP/EP)
  • Packing
  • Double polyethylene bags in HDPE drum or as per customer requirement
  • Water Content (KF)
  • Not more than 5.0%
  • Microbial Limits
  • Complies with pharmacopoeial standards
  • Endotoxins
  • < 0.25 IU/mg
  • Specific Optical Rotation
  • +82 to +88 (c=1, H2O)
 

Ceftazidime Active Pharmaceutical Ingredients Trade Information

  • Minimum Order Quantity
  • 25 Kilograms
  • Payment Terms
  • Cash on Delivery (COD), Cash Against Delivery (CAD), Cash in Advance (CID)
  • Supply Ability
  • 500 Kilograms Per Month
  • Delivery Time
  • 5-7 Days
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

About Ceftazidime Active Pharmaceutical Ingredients



Grab the latest deal on our first-string Ceftazidime Active Pharmaceutical Ingredient (API) - a ravishing choice for pharmaceutical manufacturers and suppliers. With an impeccable purity of 99% (HPLC), this white to off-white crystalline powder complies with rigorous pharmacopoeial standards and ICH Q3C guidelines. Meeting all microbial limits, it's freely soluble in water and non-sterile, specifically prepared for pharmaceutical formulations targeting bacterial infections. Packed securely in double polyethylene bags within HDPE drums, Ceftazidime ensures safety, purity, and reliability for your next innovative formulation. Don't miss this outstanding export opportunity from a trusted Indian supplier!

Ceftazidime API: Applications & Proper Usage

Ceftazidime Active Pharmaceutical Ingredient provides exceptional efficacy in the treatment of complex bacterial infections within clinical settings. It is primarily utilized in hospital and pharmaceutical manufacturing environments for producing injectables and other dosage forms. Administer the API according to recommended medicinal formulations with close adherence to pharmacopoeial guidelines. The API is processed using advanced machines guaranteeing uniform particle size (D90 <10 microns) and stable physical characteristics, making it first-string for impeccable pharmaceutical outcomes.


Payment Terms & Domestic Market Overview for Ceftazidime

Goods are shipped promptly on order confirmation, with flexible outlay options to suit wholesale and large-scale buyers. Our sample policy caters to genuine industrial inquiries, aiming to build trust with clear transaction terms. Keen focus is placed on India's robust domestic mar, ensuring timely deliveries across leading pharmaceutical zones. We support both cash and online payment systems, streamlining order processes and providing a seamless customer experience for our API clients nationwide.


FAQ's of Ceftazidime Active Pharmaceutical Ingredients:


Q: How is Ceftazidime Active Pharmaceutical Ingredient typically used?

A: Ceftazidime API is widely used in pharmaceutical manufacturing for formulating medications designed to treat serious bacterial infections. It serves as an essential component in injectables and other sterile dosage forms, following strict pharmacopoeial and safety guidelines.

Q: What are the key benefits of using this Ceftazidime API?

A: The chief benefits include impeccable purity (99%), compliance with international pharmacopeial standards, reliable stability, and safety. Its fine particle size and high solubility in water make it ideal for efficient dispersion in pharmaceutical formulations.

Q: Where should Ceftazidime API be stored to maintain its quality?

A: This API should be stored below 25C in a dry, dark, and clean environment, following manufacturer guidelines to preserve its shelf life and physical properties for up to three years.

Q: What is the process for obtaining product samples or placing a bulk order?

A: Interested buyers can request samples by contacting our sales team. Bulk orders are processed after order confirmation, and shipped goods are securely packed in HDPE drums with double polyethylene liners to ensure quality during transit.

Q: When does the product reach its expiry, and how is shelf life assured?

A: The Ceftazidime API boasts a shelf life of three years from the manufacturing date. Stability is guaranteed through carefully controlled storage conditions and packaging that meets international standards.

Q: How does the product meet international safety and quality standards?

A: Our Ceftazidime API undergoes rigorous testing for microbial limits, endotoxins, heavy metals, and residual solvents, complying fully with USP/EP and ICH Q3C guidelines, thereby assuring first-string quality and global regulatory acceptance.

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