TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva Pharmaceuticals Usa, Inc. Mexico US
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1ORCHID PHARMA LIMITED Alathur IN
04 1Ranbaxy Laboratories Limited New Delhi IN
01 4Cefadroxil monohydrate
01 3India
02 1Israel
01 3Valid
02 1Withdrawn by Holder
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2005-091 - Rev 00
Status : Valid
Issue Date : 2011-09-08
Type : Chemical
Substance Number : 813
Certificate Number : CEP 2006-203 - Rev 03
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 813
Certificate Number : CEP 2002-234 - Rev 03
Status : Valid
Issue Date : 2024-09-06
Type : Chemical
Substance Number : 813
Certificate Number : R1-CEP 1998-019 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2003-12-18
Type : Chemical
Substance Number : 813
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PharmaCompass offers a list of Cefadroxil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cefadroxil manufacturer or Cefadroxil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefadroxil manufacturer or Cefadroxil supplier.
PharmaCompass also assists you with knowing the Cefadroxil API Price utilized in the formulation of products. Cefadroxil API Price is not always fixed or binding as the Cefadroxil Price is obtained through a variety of data sources. The Cefadroxil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duracef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duracef, including repackagers and relabelers. The FDA regulates Duracef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duracef 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 Duracef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duracef supplier is an individual or a company that provides Duracef active pharmaceutical ingredient (API) or Duracef finished formulations upon request. The Duracef suppliers may include Duracef API manufacturers, exporters, distributors and traders.
click here to find a list of Duracef suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duracef CEP of the European Pharmacopoeia monograph is often referred to as a Duracef Certificate of Suitability (COS). The purpose of a Duracef CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Duracef EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Duracef to their clients by showing that a Duracef CEP has been issued for it. The manufacturer submits a Duracef CEP (COS) as part of the market authorization procedure, and it takes on the role of a Duracef CEP holder for the record. Additionally, the data presented in the Duracef CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Duracef DMF.
A Duracef CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Duracef CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Duracef suppliers with CEP (COS) on PharmaCompass.
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