01 1AUROBINDO PHARMA LIMITED Hyderabad IN
02 1FRESENIUS KABI Anti-Infectives S.r.l. Cernusco sul Naviglio IT
03 1ORCHID PHARMA LIMITED Alathur IN
01 3Cefoxitin sodium, Sterile
01 2India
02 1Italy
01 1Expired
02 1Valid
03 1Withdrawn by Holder
Certificate Number : R0-CEP 2008-015 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2013-06-10
Type : Chemical
Substance Number : 990
Certificate Number : R0-CEP 2007-173 - Rev 01
Status : Expired
Issue Date : 2013-04-24
Type : Chemical
Substance Number : 990
Certificate Number : CEP 2005-108 - Rev 06
Status : Valid
Issue Date : 2024-09-09
Type : Chemical
Substance Number : 990
A Cefoxitin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefoxitin Sodium, including repackagers and relabelers. The FDA regulates Cefoxitin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefoxitin Sodium 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 Cefoxitin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefoxitin Sodium supplier is an individual or a company that provides Cefoxitin Sodium active pharmaceutical ingredient (API) or Cefoxitin Sodium finished formulations upon request. The Cefoxitin Sodium suppliers may include Cefoxitin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cefoxitin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefoxitin Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Cefoxitin Sodium Certificate of Suitability (COS). The purpose of a Cefoxitin Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cefoxitin Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cefoxitin Sodium to their clients by showing that a Cefoxitin Sodium CEP has been issued for it. The manufacturer submits a Cefoxitin Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cefoxitin Sodium CEP holder for the record. Additionally, the data presented in the Cefoxitin Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cefoxitin Sodium DMF.
A Cefoxitin Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cefoxitin Sodium 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 Cefoxitin Sodium suppliers with CEP (COS) on PharmaCompass.
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