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01 1Fujisawa Pharmaceutical Co Ltd Osaka JP
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01 1Ceftizoxime sodium
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01 1Japan
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01 1Expired
Certificate Number : R0-CEP 2001-072 - Rev 02
Status : Expired
Issue Date : 2005-02-28
Type : TSE
Substance Number :
29
PharmaCompass offers a list of Ceftizoxime 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 Ceftizoxime Sodium manufacturer or Ceftizoxime Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ceftizoxime Sodium manufacturer or Ceftizoxime Sodium supplier.
PharmaCompass also assists you with knowing the Ceftizoxime Sodium API Price utilized in the formulation of products. Ceftizoxime Sodium API Price is not always fixed or binding as the Ceftizoxime Sodium Price is obtained through a variety of data sources. The Ceftizoxime Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CZX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CZX, including repackagers and relabelers. The FDA regulates CZX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CZX 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 CZX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CZX supplier is an individual or a company that provides CZX active pharmaceutical ingredient (API) or CZX finished formulations upon request. The CZX suppliers may include CZX API manufacturers, exporters, distributors and traders.
click here to find a list of CZX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CZX CEP of the European Pharmacopoeia monograph is often referred to as a CZX Certificate of Suitability (COS). The purpose of a CZX CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CZX EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CZX to their clients by showing that a CZX CEP has been issued for it. The manufacturer submits a CZX CEP (COS) as part of the market authorization procedure, and it takes on the role of a CZX CEP holder for the record. Additionally, the data presented in the CZX CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CZX DMF.
A CZX CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CZX 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 CZX suppliers with CEP (COS) on PharmaCompass.