01 1BASF SE Ludwigshafen DE
02 3CHONGQING HUAPONT PHARMACEUTICAL CO., LTD. Chongqing CN
03 1OLON S.P.A. Rodano IT
04 1USV PRIVATE LIMITED Mumbai IN
01 4Acitretin
02 1Acitretin, Polymorph Form-III
03 1Acitretin, Process 2
01 3China
02 1Germany
03 1India
04 1Italy
01 4Valid
02 2Withdrawn by Holder
Certificate Number : R1-CEP 2007-201 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2013-11-15
Type : Chemical
Substance Number : 1385
Certificate Number : R1-CEP 2010-038 - Rev 02
Status : Valid
Issue Date : 2018-08-17
Type : Chemical
Substance Number : 1385
Certificate Number : R0-CEP 2021-012 - Rev 00
Status : Valid
Issue Date : 2022-11-30
Type : Chemical
Substance Number : 1385
Certificate Number : R0-CEP 2005-226 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2008-02-27
Type : Chemical
Substance Number : 1385
Certificate Number : R1-CEP 2005-186 - Rev 08
Status : Valid
Issue Date : 2023-05-25
Type : Chemical
Substance Number : 1385
Certificate Number : CEP 2022-387 - Rev 00
Status : Valid
Issue Date : 2024-10-24
Type : Chemical
Substance Number : 1385
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PharmaCompass offers a list of Acitretin 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 Acitretin manufacturer or Acitretin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acitretin manufacturer or Acitretin supplier.
PharmaCompass also assists you with knowing the Acitretin API Price utilized in the formulation of products. Acitretin API Price is not always fixed or binding as the Acitretin Price is obtained through a variety of data sources. The Acitretin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etretin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etretin, including repackagers and relabelers. The FDA regulates Etretin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etretin 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 Etretin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etretin supplier is an individual or a company that provides Etretin active pharmaceutical ingredient (API) or Etretin finished formulations upon request. The Etretin suppliers may include Etretin API manufacturers, exporters, distributors and traders.
click here to find a list of Etretin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etretin CEP of the European Pharmacopoeia monograph is often referred to as a Etretin Certificate of Suitability (COS). The purpose of a Etretin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etretin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etretin to their clients by showing that a Etretin CEP has been issued for it. The manufacturer submits a Etretin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etretin CEP holder for the record. Additionally, the data presented in the Etretin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etretin DMF.
A Etretin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etretin 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 Etretin suppliers with CEP (COS) on PharmaCompass.
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