01 1S.P. QUIMICA, S.A. Riudoms ES
02 1Suzhou No.5 Pharmaceutical Factory Co., Ltd. Suzhou CN
01 2Nifuroxazide
01 1China
02 1Spain
01 1Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 2009-003 - Rev 00
Status : Valid
Issue Date : 2015-06-26
Type : Chemical
Substance Number : 1999
Certificate Number : R0-CEP 2006-074 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-05-06
Type : Chemical
Substance Number : 1999
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PharmaCompass offers a list of Nifuroxazide 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 Nifuroxazide manufacturer or Nifuroxazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nifuroxazide manufacturer or Nifuroxazide supplier.
PharmaCompass also assists you with knowing the Nifuroxazide API Price utilized in the formulation of products. Nifuroxazide API Price is not always fixed or binding as the Nifuroxazide Price is obtained through a variety of data sources. The Nifuroxazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eskapar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eskapar, including repackagers and relabelers. The FDA regulates Eskapar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eskapar 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 Eskapar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eskapar supplier is an individual or a company that provides Eskapar active pharmaceutical ingredient (API) or Eskapar finished formulations upon request. The Eskapar suppliers may include Eskapar API manufacturers, exporters, distributors and traders.
click here to find a list of Eskapar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eskapar CEP of the European Pharmacopoeia monograph is often referred to as a Eskapar Certificate of Suitability (COS). The purpose of a Eskapar CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Eskapar EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Eskapar to their clients by showing that a Eskapar CEP has been issued for it. The manufacturer submits a Eskapar CEP (COS) as part of the market authorization procedure, and it takes on the role of a Eskapar CEP holder for the record. Additionally, the data presented in the Eskapar CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Eskapar DMF.
A Eskapar CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Eskapar 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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