01 Ajinomoto Co., Inc. Tokyo JP (1)
02 DAIICHI SANKYO CHEMICAL PHARMA CO., LTD. Kanagawa JP (1)
03 DIVI'S LABORATORIES LIMITED Hyderabad IN (1)
04 EGIS Pharmaceuticals PLC Budapest HU (1)
05 GUANGXI BONGER PHARMACEUTICAL CO., LTD. Tiandong Town CN (1)
06 HETERO DRUGS LIMITED Hyderabad IN (1)
07 MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN (1)
08 SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN (1)
09 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (2)
10 TORRENT PHARMACEUTICALS LIMITED Village Bhat IN (1)
11 ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN (1)
12 ZHEJIANG WILD WIND PHARMACEUTICAL CO., LTD. Geshan Town CN (2)
01 Levodopa (12)
02 Levodopa, Enzymatic process (2)
01 China (4)
02 Hungary (1)
03 India (4)
04 Israel (2)
05 Japan (2)
06 Blank (1)
01 Valid (12)
02 Withdrawn by Holder (2)
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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 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.
We have 11 companies offering Etilevodopa
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