01 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
02 1Bayer Hispania, S.L. La Felguera ES
03 1Erregierre S.p.A. San Paolo D'Argon IT
04 1F.I.S. - Fabbrica Italiana Sintetici S.p.A. Montecchio Maggiore IT
05 1OLON S.P.A. Rodano IT
01 4Clotrimazole
02 1Clotrimazole, Standard and micronised grade
01 1Germany
02 1India
03 3Italy
01 5Valid
Certificate Number : R1-CEP 2000-009 - Rev 01
Status : Valid
Issue Date : 2019-10-07
Type : Chemical
Substance Number : 757
Certificate Number : R1-CEP 2003-187 - Rev 02
Status : Valid
Issue Date : 2011-07-28
Type : Chemical
Substance Number : 757
Certificate Number : CEP 2005-176 - Rev 03
Status : Valid
Issue Date : 2024-01-31
Type : Chemical
Substance Number : 757
Clotrimazole, Standard And Micronised Grade
Certificate Number : CEP 2008-326 - Rev 03
Status : Valid
Issue Date : 2024-07-03
Type : Chemical
Substance Number : 757
Certificate Number : CEP 2004-102 - Rev 06
Status : Valid
Issue Date : 2025-03-24
Type : Chemical
Substance Number : 757
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PharmaCompass offers a list of Clotrimazole 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 Clotrimazole manufacturer or Clotrimazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clotrimazole manufacturer or Clotrimazole supplier.
PharmaCompass also assists you with knowing the Clotrimazole API Price utilized in the formulation of products. Clotrimazole API Price is not always fixed or binding as the Clotrimazole Price is obtained through a variety of data sources. The Clotrimazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Canestene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Canestene, including repackagers and relabelers. The FDA regulates Canestene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Canestene 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 Canestene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Canestene supplier is an individual or a company that provides Canestene active pharmaceutical ingredient (API) or Canestene finished formulations upon request. The Canestene suppliers may include Canestene API manufacturers, exporters, distributors and traders.
click here to find a list of Canestene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Canestene CEP of the European Pharmacopoeia monograph is often referred to as a Canestene Certificate of Suitability (COS). The purpose of a Canestene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Canestene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Canestene to their clients by showing that a Canestene CEP has been issued for it. The manufacturer submits a Canestene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Canestene CEP holder for the record. Additionally, the data presented in the Canestene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Canestene DMF.
A Canestene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Canestene 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 Canestene suppliers with CEP (COS) on PharmaCompass.
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