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 : R1-CEP 2004-102 - Rev 05
Status : Valid
Issue Date : 2020-12-01
Type : Chemical
Substance Number : 757
A Lotrimin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lotrimin, including repackagers and relabelers. The FDA regulates Lotrimin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lotrimin 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 Lotrimin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lotrimin supplier is an individual or a company that provides Lotrimin active pharmaceutical ingredient (API) or Lotrimin finished formulations upon request. The Lotrimin suppliers may include Lotrimin API manufacturers, exporters, distributors and traders.
click here to find a list of Lotrimin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lotrimin CEP of the European Pharmacopoeia monograph is often referred to as a Lotrimin Certificate of Suitability (COS). The purpose of a Lotrimin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lotrimin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lotrimin to their clients by showing that a Lotrimin CEP has been issued for it. The manufacturer submits a Lotrimin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lotrimin CEP holder for the record. Additionally, the data presented in the Lotrimin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lotrimin DMF.
A Lotrimin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lotrimin 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 Lotrimin suppliers with CEP (COS) on PharmaCompass.
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