Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1CENTRIENT PHARMACEUTICALS NETHERLANDS B.V. Delft NL
02 1DSM Anti-Infectives Chemferm SA Santa Perpétua De Mogoda ES
03 1ORCHID PHARMA LIMITED Alathur IN
04 1Ranbaxy Laboratories Limited New Delhi IN
01 3Cefradine
02 1Cefradine, Enzymatic process
01 2India
02 2Netherlands
01 2Valid
02 2Withdrawn by Holder
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Certificate Number : R1-CEP 2005-181 - Rev 03
Status : Valid
Issue Date : 2019-09-09
Type : Chemical
Substance Number : 814
Certificate Number : CEP 2002-231 - Rev 04
Status : Valid
Issue Date : 2024-09-06
Type : Chemical
Substance Number : 814
Certificate Number : R1-CEP 1997-106 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2004-01-06
Type : Chemical
Substance Number : 814
Certificate Number : R1-CEP 1997-116 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2006-06-28
Type : Chemical
Substance Number : 814
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PharmaCompass offers a list of Cephradine 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 Cephradine manufacturer or Cephradine supplier for your needs.
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PharmaCompass also assists you with knowing the Cephradine API Price utilized in the formulation of products. Cephradine API Price is not always fixed or binding as the Cephradine Price is obtained through a variety of data sources. The Cephradine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cephradine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cephradine, including repackagers and relabelers. The FDA regulates Cephradine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cephradine 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 Cephradine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cephradine supplier is an individual or a company that provides Cephradine active pharmaceutical ingredient (API) or Cephradine finished formulations upon request. The Cephradine suppliers may include Cephradine API manufacturers, exporters, distributors and traders.
click here to find a list of Cephradine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cephradine CEP of the European Pharmacopoeia monograph is often referred to as a Cephradine Certificate of Suitability (COS). The purpose of a Cephradine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cephradine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cephradine to their clients by showing that a Cephradine CEP has been issued for it. The manufacturer submits a Cephradine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cephradine CEP holder for the record. Additionally, the data presented in the Cephradine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cephradine DMF.
A Cephradine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cephradine 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 Cephradine suppliers with CEP (COS) on PharmaCompass.
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