IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
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01 1IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 1Moehs Iberica S.L. Rubi ES
03 1AALIDHRA PHARMACHEM PRIVATE LIMITED Nandesari IN
04 2ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
05 1CORDEN PHARMA CHENOVE CHENOVE FR
06 1D. K. PHARMA CHEM PRIVATE LIMITED Badlapur IN
07 1DERIVADOS QUIMICOS S.A.U. Alcantarilla ES
08 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
09 1HARMAN FINOCHEM LIMITED Mumbai IN
10 1HETERO DRUGS LIMITED Hyderabad IN
11 1IPCA Laboratories Limited Mumbai IN
12 1JIANGSU NHWA PHARMACEUTICAL CO., LTD. Xuzhou City CN
13 1Nexchem Pharmaceutical Co., Ltd. Jinhua City CN
14 2OLON S.P.A. Rodano IT
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01 14Fenofibrate
02 1Fenofibrate, Non-micronised, micronised
03 1Fenofibrate, Process-II
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01 2China
02 1Germany
03 9India
04 2Italy
05 2Spain
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01 1Expired
02 14Valid
03 1Withdrawn by Holder
Certificate Number : CEP 2018-075 - Rev 03
Status : Valid
Issue Date : 2023-11-02
Type : Chemical
Substance Number : 1322
Certificate Number : CEP 1998-128 - Rev 08
Status : Valid
Issue Date : 2023-09-07
Type : Chemical
Substance Number : 1322
Certificate Number : R1-CEP 2016-017 - Rev 00
Status : Valid
Issue Date : 2021-11-19
Type : Chemical
Substance Number : 1322
Certificate Number : R1-CEP 2001-314 - Rev 02
Status : Valid
Issue Date : 2018-01-29
Type : Chemical
Substance Number : 1322
Certificate Number : R1-CEP 2016-036 - Rev 00
Status : Valid
Issue Date : 2023-01-11
Type : Chemical
Substance Number : 1322
Certificate Number : CEP 2020-213 - Rev 01
Status : Valid
Issue Date : 2024-08-21
Type : Chemical
Substance Number : 1322
Certificate Number : CEP 2012-290 - Rev 02
Status : Valid
Issue Date : 2025-07-07
Type : Chemical
Substance Number : 1322
Certificate Number : CEP 2007-350 - Rev 02
Status : Valid
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 1322
Certificate Number : R1-CEP 2001-178 - Rev 04
Status : Valid
Issue Date : 2022-06-15
Type : Chemical
Substance Number : 1322
Certificate Number : R1-CEP 2003-260 - Rev 05
Status : Valid
Issue Date : 2022-03-29
Type : Chemical
Substance Number : 1322
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PharmaCompass offers a list of Fenofibrate 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 Fenofibrate manufacturer or Fenofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fenofibrate manufacturer or Fenofibrate supplier.
PharmaCompass also assists you with knowing the Fenofibrate API Price utilized in the formulation of products. Fenofibrate API Price is not always fixed or binding as the Fenofibrate Price is obtained through a variety of data sources. The Fenofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenofibrate MSD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenofibrate MSD, including repackagers and relabelers. The FDA regulates Fenofibrate MSD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenofibrate MSD 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 Fenofibrate MSD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenofibrate MSD supplier is an individual or a company that provides Fenofibrate MSD active pharmaceutical ingredient (API) or Fenofibrate MSD finished formulations upon request. The Fenofibrate MSD suppliers may include Fenofibrate MSD API manufacturers, exporters, distributors and traders.
click here to find a list of Fenofibrate MSD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fenofibrate MSD CEP of the European Pharmacopoeia monograph is often referred to as a Fenofibrate MSD Certificate of Suitability (COS). The purpose of a Fenofibrate MSD CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fenofibrate MSD EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fenofibrate MSD to their clients by showing that a Fenofibrate MSD CEP has been issued for it. The manufacturer submits a Fenofibrate MSD CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fenofibrate MSD CEP holder for the record. Additionally, the data presented in the Fenofibrate MSD CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fenofibrate MSD DMF.
A Fenofibrate MSD CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fenofibrate MSD 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 Fenofibrate MSD suppliers with CEP (COS) on PharmaCompass.
We have 14 companies offering Fenofibrate MSD
Get in contact with the supplier of your choice: