01 1Ajinomoto Co., Inc. Tokyo JP
02 1DAIICHI SANKYO CHEMICAL PHARMA CO., LTD. Kanagawa JP
03 1DIVI'S LABORATORIES LIMITED Hyderabad IN
04 1GUANGXI BONGER PHARMACEUTICAL CO., LTD. Tiandong Town CN
05 1HETERO DRUGS LIMITED Hyderabad IN
06 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
07 1SHANDONG LUKANG PHARMACEUTICAL CO., LTD. Jining City CN
08 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
09 2TAPI NL B.V. Amsterdam NL
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 5China
02 4India
03 2Japan
04 3Blank
01 12Valid
02 2Withdrawn by Holder
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 2022-320 - Rev 00
Status : Valid
Issue Date : 2023-03-14
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 : CEP 2017-090 - Rev 04
Status : Valid
Issue Date : 2024-04-24
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
Certificate Number : R1-CEP 2012-377 - Rev 00
Status : Valid
Issue Date : 2019-02-28
Type : Chemical
Substance Number : 38
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Product Web Link
Virtual Booth
Digital Content
Website
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2013-293 - Rev 02
Status : Valid
Issue Date : 2025-02-27
Type : Chemical
Substance Number : 38
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
62
PharmaCompass offers a list of Etilevodopa 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 Etilevodopa manufacturer or Etilevodopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etilevodopa manufacturer or Etilevodopa supplier.
PharmaCompass also assists you with knowing the Etilevodopa API Price utilized in the formulation of products. Etilevodopa API Price is not always fixed or binding as the Etilevodopa Price is obtained through a variety of data sources. The Etilevodopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ledopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ledopa, including repackagers and relabelers. The FDA regulates Ledopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ledopa 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 Ledopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ledopa supplier is an individual or a company that provides Ledopa active pharmaceutical ingredient (API) or Ledopa finished formulations upon request. The Ledopa suppliers may include Ledopa API manufacturers, exporters, distributors and traders.
click here to find a list of Ledopa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ledopa CEP of the European Pharmacopoeia monograph is often referred to as a Ledopa Certificate of Suitability (COS). The purpose of a Ledopa CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ledopa EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ledopa to their clients by showing that a Ledopa CEP has been issued for it. The manufacturer submits a Ledopa CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ledopa CEP holder for the record. Additionally, the data presented in the Ledopa CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ledopa DMF.
A Ledopa CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ledopa 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 Ledopa suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Ledopa
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