01 1CHIFENG PHARMACEUTICAL CO., LTD. Chifeng CN
02 1Glaxo Wellcome London GB
01 2Griseofulvin
01 1China
02 1United Kingdom
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2000-374 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2001-11-21
Type : TSE
Substance Number : 182
Certificate Number : R1-CEP 2002-143 - Rev 02
Status : Valid
Issue Date : 2022-11-07
Type : Chemical
Substance Number : 182
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PharmaCompass offers a list of Griseofulvin 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 Griseofulvin manufacturer or Griseofulvin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Griseofulvin manufacturer or Griseofulvin supplier.
PharmaCompass also assists you with knowing the Griseofulvin API Price utilized in the formulation of products. Griseofulvin API Price is not always fixed or binding as the Griseofulvin Price is obtained through a variety of data sources. The Griseofulvin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A M542 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of M542, including repackagers and relabelers. The FDA regulates M542 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. M542 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 M542 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A M542 supplier is an individual or a company that provides M542 active pharmaceutical ingredient (API) or M542 finished formulations upon request. The M542 suppliers may include M542 API manufacturers, exporters, distributors and traders.
click here to find a list of M542 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A M542 CEP of the European Pharmacopoeia monograph is often referred to as a M542 Certificate of Suitability (COS). The purpose of a M542 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of M542 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of M542 to their clients by showing that a M542 CEP has been issued for it. The manufacturer submits a M542 CEP (COS) as part of the market authorization procedure, and it takes on the role of a M542 CEP holder for the record. Additionally, the data presented in the M542 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the M542 DMF.
A M542 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. M542 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 M542 suppliers with CEP (COS) on PharmaCompass.
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