IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1PHARMASYNTHESE Saint Pierre Les Elbeuf FR
02 1PMC ISOCHEM Vert Le Petit FR
03 2OPTIMUS DRUGS PRIVATE LIMITED Hyderabad IN
04 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
01 3Fenticonazole nitrate
02 1Fenticonazole nitrate, FCZ code process
03 1Fenticonazole nitrate, Micronised
01 2France
02 2India
03 1Italy
01 4Valid
02 1Withdrawn by Holder
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Fenticonazole Nitrate, Micronised
Certificate Number : CEP 2015-157 - Rev 01
Status : Valid
Issue Date : 2024-03-20
Type : Chemical
Substance Number : 1211
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
Certificate Number : CEP 2015-291 - Rev 01
Status : Valid
Issue Date : 2024-04-10
Type : Chemical
Substance Number : 1211
Fenticonazole Nitrate, FCZ Code Process
Certificate Number : CEP 2020-046 - Rev 02
Status : Valid
Issue Date : 2024-03-04
Type : Chemical
Substance Number : 1211
Certificate Number : R1-CEP 2013-056 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2019-10-24
Type : Chemical
Substance Number : 1211
Certificate Number : CEP 2014-374 - Rev 01
Status : Valid
Issue Date : 2024-04-17
Type : Chemical
Substance Number : 1211
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PharmaCompass offers a list of Fenticonazole Nitrate 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 Fenticonazole Nitrate manufacturer or Fenticonazole Nitrate supplier for your needs.
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A Lomexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomexin, including repackagers and relabelers. The FDA regulates Lomexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomexin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lomexin supplier is an individual or a company that provides Lomexin active pharmaceutical ingredient (API) or Lomexin finished formulations upon request. The Lomexin suppliers may include Lomexin API manufacturers, exporters, distributors and traders.
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A Lomexin CEP of the European Pharmacopoeia monograph is often referred to as a Lomexin Certificate of Suitability (COS). The purpose of a Lomexin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lomexin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lomexin to their clients by showing that a Lomexin CEP has been issued for it. The manufacturer submits a Lomexin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lomexin CEP holder for the record. Additionally, the data presented in the Lomexin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lomexin DMF.
A Lomexin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lomexin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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