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Status : Withdrawn by Holder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Status : Withdrawn by Holder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