TAPI offers customized CDMO Solutions for API development and manufacturing services.
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 offers customized CDMO Solutions for API development and manufacturing services.
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
A Methyldopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyldopa, including repackagers and relabelers. The FDA regulates Methyldopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyldopa 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 Methyldopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyldopa supplier is an individual or a company that provides Methyldopa active pharmaceutical ingredient (API) or Methyldopa finished formulations upon request. The Methyldopa suppliers may include Methyldopa API manufacturers, exporters, distributors and traders.
click here to find a list of Methyldopa 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 Methyldopa Drug Master File in Japan (Methyldopa JDMF) empowers Methyldopa 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 Methyldopa JDMF during the approval evaluation for pharmaceutical products. At the time of Methyldopa 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 Methyldopa suppliers with JDMF on PharmaCompass.
We have 3 companies offering Methyldopa
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