Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1TRANSO-PHARM HANDELS GMBH Siek DE
02 1Bidachem S.p.A. Fornovo San Giovanni IT
03 1MIDAS PHARMA GMBH Ingelheim am Rhein DE
01 3Crotamiton
01 2Germany
02 1Italy
01 2Valid
02 1Withdrawn by Holder
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Certificate Number : CEP 2014-260 - Rev 01
Status : Valid
Issue Date : 2024-11-15
Type : Chemical
Substance Number : 1194
Certificate Number : R1-CEP 1999-131 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2012-05-11
Type : Chemical
Substance Number : 1194
Certificate Number : CEP 2018-095 - Rev 03
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 1194
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PharmaCompass offers a list of Crotamiton API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Crotamiton manufacturer or Crotamiton supplier for your needs.
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A 483-63-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 483-63-6, including repackagers and relabelers. The FDA regulates 483-63-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 483-63-6 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 483-63-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 483-63-6 supplier is an individual or a company that provides 483-63-6 active pharmaceutical ingredient (API) or 483-63-6 finished formulations upon request. The 483-63-6 suppliers may include 483-63-6 API manufacturers, exporters, distributors and traders.
click here to find a list of 483-63-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A 483-63-6 CEP of the European Pharmacopoeia monograph is often referred to as a 483-63-6 Certificate of Suitability (COS). The purpose of a 483-63-6 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 483-63-6 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 483-63-6 to their clients by showing that a 483-63-6 CEP has been issued for it. The manufacturer submits a 483-63-6 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 483-63-6 CEP holder for the record. Additionally, the data presented in the 483-63-6 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 483-63-6 DMF.
A 483-63-6 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 483-63-6 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 483-63-6 suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering 483-63-6
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