TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 2TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
02 1Ajinomoto Co., Inc. Tokyo JP
03 1DAIICHI SANKYO CHEMICAL PHARMA CO., LTD. Kanagawa JP
04 1DIVI'S LABORATORIES LIMITED Hyderabad IN
05 1EGIS Pharmaceuticals PLC Budapest HU
06 1GUANGXI BONGER PHARMACEUTICAL CO., LTD. Tiandong Town CN
07 1HETERO DRUGS LIMITED Hyderabad IN
08 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
09 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
10 1TORRENT PHARMACEUTICALS LIMITED Village Bhat IN
11 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
12 2ZHEJIANG WILD WIND PHARMACEUTICAL CO., LTD. Geshan Town CN
01 12Levodopa
02 2Levodopa, Enzymatic process
01 4China
02 1Hungary
03 4India
04 2Israel
05 2Japan
06 1Blank
01 11Valid
02 3Withdrawn by Holder
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 1999-187 - Rev 09
Status : Valid
Issue Date : 2022-03-24
Type : Chemical
Substance Number : 38
Certificate Number : R1-CEP 1999-001 - Rev 01
Status : Valid
Issue Date : 2007-10-19
Type : Chemical
Substance Number : 38
Certificate Number : R1-CEP 2005-161 - Rev 04
Status : Valid
Issue Date : 2018-01-25
Type : Chemical
Substance Number : 38
Certificate Number : R0-CEP 2020-161 - Rev 00
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 38
Certificate Number : R1-CEP 2009-174 - Rev 02
Status : Valid
Issue Date : 2022-04-11
Type : Chemical
Substance Number : 38
Certificate Number : R1-CEP 2013-293 - Rev 01
Status : Valid
Issue Date : 2021-11-22
Type : Chemical
Substance Number : 38
Certificate Number : CEP 2017-090 - Rev 04
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 38
Certificate Number : R1-CEP 2012-377 - Rev 00
Status : Valid
Issue Date : 2019-02-28
Type : Chemical
Substance Number : 38
Certificate Number : R0-CEP 2021-195 - Rev 00
Status : Valid
Issue Date : 2022-10-12
Type : Chemical
Substance Number : 38
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Product Web Link
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Corporate PDF
Certificate Number : R1-CEP 2014-348 - Rev 00
Status : Valid
Issue Date : 2021-09-17
Type : Chemical
Substance Number : 38
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Etilevodopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etilevodopa, including repackagers and relabelers. The FDA regulates Etilevodopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etilevodopa 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 Etilevodopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etilevodopa supplier is an individual or a company that provides Etilevodopa active pharmaceutical ingredient (API) or Etilevodopa finished formulations upon request. The Etilevodopa suppliers may include Etilevodopa API manufacturers, exporters, distributors and traders.
click here to find a list of Etilevodopa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etilevodopa CEP of the European Pharmacopoeia monograph is often referred to as a Etilevodopa Certificate of Suitability (COS). The purpose of a Etilevodopa CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etilevodopa EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etilevodopa to their clients by showing that a Etilevodopa CEP has been issued for it. The manufacturer submits a Etilevodopa CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etilevodopa CEP holder for the record. Additionally, the data presented in the Etilevodopa CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etilevodopa DMF.
A Etilevodopa CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etilevodopa 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 Etilevodopa suppliers with CEP (COS) on PharmaCompass.
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