01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1HIKAL LIMITED Bangalore IN
03 1Recordati S.p.A. Milano IT
04 1TAPI NL B.V. Amsterdam NL
05 1ZHEJIANG EXCEL PHARMACEUTICAL CO., LTD. Taizhou CN
01 5Gemfibrozil
01 1China
02 2India
03 1Italy
04 1Blank
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 2008-118 - Rev 01
Status : Valid
Issue Date : 2021-09-20
Type : Chemical
Substance Number : 1694
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2006-210 - Rev 06
Status : Valid
Issue Date : 2025-07-15
Type : Chemical
Substance Number : 1694
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
41
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 CI 719 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 719, including repackagers and relabelers. The FDA regulates CI 719 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 719 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 CI 719 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CI 719 supplier is an individual or a company that provides CI 719 active pharmaceutical ingredient (API) or CI 719 finished formulations upon request. The CI 719 suppliers may include CI 719 API manufacturers, exporters, distributors and traders.
click here to find a list of CI 719 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CI 719 CEP of the European Pharmacopoeia monograph is often referred to as a CI 719 Certificate of Suitability (COS). The purpose of a CI 719 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CI 719 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CI 719 to their clients by showing that a CI 719 CEP has been issued for it. The manufacturer submits a CI 719 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CI 719 CEP holder for the record. Additionally, the data presented in the CI 719 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CI 719 DMF.
A CI 719 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CI 719 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 CI 719 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering CI 719
Get in contact with the supplier of your choice:
