01 1Zhejiang Chiral Medicine Chemicals Co. , Ltd.
02 1Zhejiang Wild Wind Pharmaceutical Co. , Ltd.
01 2Methyldopa hydrate
01 2China
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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Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methyldopa manufacturer or Methyldopa supplier.
A Aldomet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aldomet, including repackagers and relabelers. The FDA regulates Aldomet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aldomet 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 Aldomet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Aldomet supplier is an individual or a company that provides Aldomet active pharmaceutical ingredient (API) or Aldomet finished formulations upon request. The Aldomet suppliers may include Aldomet API manufacturers, exporters, distributors and traders.
click here to find a list of Aldomet suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Aldomet Drug Master File in Japan (Aldomet JDMF) empowers Aldomet 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 Aldomet JDMF during the approval evaluation for pharmaceutical products. At the time of Aldomet 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 Aldomet suppliers with JDMF on PharmaCompass.
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