01 1FRESENIUS KABI IPSUM S.R.L. Cassina de’ Pecchi IT
02 1Qilu Antibiotics Pharmaceutical Co., Ltd. Jinan CN
01 2Cefoperazone sodium, Sterile
01 1China
02 1Italy
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2003-277 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2021-02-10
Type : Chemical
Substance Number : 1404
Certificate Number : CEP 2007-202 - Rev 04
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 1404
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PharmaCompass offers a list of Cefoperazone Sodium 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 Cefoperazone Sodium manufacturer or Cefoperazone Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Cefoperazone Sodium API Price utilized in the formulation of products. Cefoperazone Sodium API Price is not always fixed or binding as the Cefoperazone Sodium Price is obtained through a variety of data sources. The Cefoperazone Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefobid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefobid, including repackagers and relabelers. The FDA regulates Cefobid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefobid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Cefobid supplier is an individual or a company that provides Cefobid active pharmaceutical ingredient (API) or Cefobid finished formulations upon request. The Cefobid suppliers may include Cefobid API manufacturers, exporters, distributors and traders.
click here to find a list of Cefobid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefobid CEP of the European Pharmacopoeia monograph is often referred to as a Cefobid Certificate of Suitability (COS). The purpose of a Cefobid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cefobid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cefobid to their clients by showing that a Cefobid CEP has been issued for it. The manufacturer submits a Cefobid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cefobid CEP holder for the record. Additionally, the data presented in the Cefobid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cefobid DMF.
A Cefobid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cefobid CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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