TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva Pharmaceutical & Chemical (Hangzhou) Co. , Ltd.
02 1Zhejiang Chiral Medicine Chemicals Co. , Ltd.
03 1Zhejiang Wild Wind Pharmaceutical Co. , Ltd.
01 1Methyldopa "Teva"
02 2Methyldopa hydrate
01 2China
02 1Israel
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 227MF10141
Registrant's Address : No. 1889, Jingliu Road, Linjiang Industrial Zone, Qiantang New District, Hangzhou, Ch...
Initial Date of Registration : 2015-05-14
Latest Date of Registration : 2015-05-14
Registration Number : 306MF10095
Registrant's Address : Nanyang Economy Development Zone, Xiaoshan, Hangzhou, Zhejiang, China
Initial Date of Registration : 2024-07-11
Latest Date of Registration : 2024-07-11
Registration Number : 226MF10099
Registrant's Address : Beijing Industrial Zone, Geshan Town, Dongyang, Zhejiang Province, China
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2014-05-14
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PharmaCompass offers a list of Methyldopa 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 Methyldopa manufacturer or Methyldopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methyldopa manufacturer or Methyldopa supplier.
PharmaCompass also assists you with knowing the Methyldopa API Price utilized in the formulation of products. Methyldopa API Price is not always fixed or binding as the Methyldopa Price is obtained through a variety of data sources. The Methyldopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dopamet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dopamet, including repackagers and relabelers. The FDA regulates Dopamet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dopamet 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 Dopamet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dopamet supplier is an individual or a company that provides Dopamet active pharmaceutical ingredient (API) or Dopamet finished formulations upon request. The Dopamet suppliers may include Dopamet API manufacturers, exporters, distributors and traders.
click here to find a list of Dopamet 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 Dopamet Drug Master File in Japan (Dopamet JDMF) empowers Dopamet 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 Dopamet JDMF during the approval evaluation for pharmaceutical products. At the time of Dopamet JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Dopamet suppliers with JDMF on PharmaCompass.
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