IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
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
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : CEP 2018-075 - Rev 03
Status : Valid
Issue Date : 2023-11-02
Type : Chemical
Substance Number : 1322
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 1998-128 - Rev 08
Status : Valid
Issue Date : 2023-09-07
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.
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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 EU-0100486 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EU-0100486, including repackagers and relabelers. The FDA regulates EU-0100486 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EU-0100486 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 EU-0100486 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EU-0100486 supplier is an individual or a company that provides EU-0100486 active pharmaceutical ingredient (API) or EU-0100486 finished formulations upon request. The EU-0100486 suppliers may include EU-0100486 API manufacturers, exporters, distributors and traders.
click here to find a list of EU-0100486 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EU-0100486 CEP of the European Pharmacopoeia monograph is often referred to as a EU-0100486 Certificate of Suitability (COS). The purpose of a EU-0100486 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of EU-0100486 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of EU-0100486 to their clients by showing that a EU-0100486 CEP has been issued for it. The manufacturer submits a EU-0100486 CEP (COS) as part of the market authorization procedure, and it takes on the role of a EU-0100486 CEP holder for the record. Additionally, the data presented in the EU-0100486 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the EU-0100486 DMF.
A EU-0100486 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. EU-0100486 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 EU-0100486 suppliers with CEP (COS) on PharmaCompass.
We have 14 companies offering EU-0100486
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