01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1HIKAL LIMITED Bangalore IN
03 1Recordati S.p.A. Milano IT
04 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
05 1ZHEJIANG EXCEL PHARMACEUTICAL CO., LTD. Taizhou CN
01 5Gemfibrozil
01 1China
02 2India
03 1Israel
04 1Italy
01 1Expired
02 4Valid
Certificate Number : CEP 2006-221 - Rev 05
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 1694
Certificate Number : R1-CEP 2007-089 - Rev 05
Status : Valid
Issue Date : 2022-09-07
Type : Chemical
Substance Number : 1694
Certificate Number : R0-CEP 2009-189 - Rev 00
Status : Expired
Issue Date : 2010-09-15
Type : Chemical
Substance Number : 1694
Certificate Number : R1-CEP 2006-210 - Rev 05
Status : Valid
Issue Date : 2022-01-05
Type : Chemical
Substance Number : 1694
Certificate Number : R1-CEP 2008-118 - Rev 01
Status : Valid
Issue Date : 2021-09-20
Type : Chemical
Substance Number : 1694
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PharmaCompass offers a list of Gemfibrozil 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 Gemfibrozil manufacturer or Gemfibrozil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gemfibrozil manufacturer or Gemfibrozil supplier.
PharmaCompass also assists you with knowing the Gemfibrozil API Price utilized in the formulation of products. Gemfibrozil API Price is not always fixed or binding as the Gemfibrozil Price is obtained through a variety of data sources. The Gemfibrozil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gevilon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gevilon, including repackagers and relabelers. The FDA regulates Gevilon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gevilon 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 Gevilon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gevilon supplier is an individual or a company that provides Gevilon active pharmaceutical ingredient (API) or Gevilon finished formulations upon request. The Gevilon suppliers may include Gevilon API manufacturers, exporters, distributors and traders.
click here to find a list of Gevilon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gevilon CEP of the European Pharmacopoeia monograph is often referred to as a Gevilon Certificate of Suitability (COS). The purpose of a Gevilon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gevilon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gevilon to their clients by showing that a Gevilon CEP has been issued for it. The manufacturer submits a Gevilon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gevilon CEP holder for the record. Additionally, the data presented in the Gevilon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gevilon DMF.
A Gevilon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gevilon 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 Gevilon suppliers with CEP (COS) on PharmaCompass.
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