01 2Ajinomoto Co., Inc.
02 1DIVI'S LABORATORIES LIMITED
03 1Shandong Xinhua Pharmaceutical Co. , Ltd.
01 2Japanese Pharmacopoeia levodopa (production only)
02 1L-Dihydroxyphenylalanine
03 1Levodopa
01 1China
02 1India
03 2Japan
Registration Number : 302MF10140
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-11-26
Latest Date of Registration : 2020-11-26
Japanese Pharmacopoeia Levodopa (for manufacturing purposes only)
Registration Number : 221MF10284
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2009-12-22
Latest Date of Registration : 2009-12-22
Registration Number : 227MF10235
Registrant's Address : 1-72/23(P)/DIVIS/303, Divi Towers, Cyber Hills, Gachibowli, Hyderabad-500 032, ...
Initial Date of Registration : 2015-09-24
Latest Date of Registration : 2018-04-12
Japanese Pharmacopoeia Levodopa (for manufacturing purposes only)
Registration Number : 221MF10029
Registrant's Address : No. 1, Lutai Road, High-tech District, Zibo, Shandong, P. R. China
Initial Date of Registration : 2009-02-09
Latest Date of Registration : 2009-02-09
20
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.
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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 DAH manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DAH, including repackagers and relabelers. The FDA regulates DAH manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DAH 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 DAH manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DAH supplier is an individual or a company that provides DAH active pharmaceutical ingredient (API) or DAH finished formulations upon request. The DAH suppliers may include DAH API manufacturers, exporters, distributors and traders.
click here to find a list of DAH suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The DAH Drug Master File in Japan (DAH JDMF) empowers DAH API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the DAH JDMF during the approval evaluation for pharmaceutical products. At the time of DAH JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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