01 2Aurobindo Pharma Limited
02 1Covalent Laboratories Private Limited
03 1PURE AND CURE HEALTHCARE PRIVATE LIMITED
01 1CEFUROXIME AXETIL
02 2Cefuroxime Axetil
03 1Cefuroxime axetil
01 3India
02 1Blank
NDC Package Code : 65862-505
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-339
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61788-1000
Start Marketing Date : 2015-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82608-008
Start Marketing Date : 2022-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Cefuroxime Axetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxime Axetil, including repackagers and relabelers. The FDA regulates Cefuroxime Axetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxime Axetil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cefuroxime Axetil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefuroxime Axetil supplier is an individual or a company that provides Cefuroxime Axetil active pharmaceutical ingredient (API) or Cefuroxime Axetil finished formulations upon request. The Cefuroxime Axetil suppliers may include Cefuroxime Axetil API manufacturers, exporters, distributors and traders.
click here to find a list of Cefuroxime Axetil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Cefuroxime Axetil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cefuroxime Axetil API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Cefuroxime Axetil as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Cefuroxime Axetil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cefuroxime Axetil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cefuroxime Axetil suppliers with NDC on PharmaCompass.
We have 2 companies offering Cefuroxime Axetil
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
