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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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.
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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 Methyldopa Alphapharm Brand manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyldopa Alphapharm Brand, including repackagers and relabelers. The FDA regulates Methyldopa Alphapharm Brand manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyldopa Alphapharm Brand API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Methyldopa Alphapharm Brand supplier is an individual or a company that provides Methyldopa Alphapharm Brand active pharmaceutical ingredient (API) or Methyldopa Alphapharm Brand finished formulations upon request. The Methyldopa Alphapharm Brand suppliers may include Methyldopa Alphapharm Brand API manufacturers, exporters, distributors and traders.
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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 Alphapharm Brand Drug Master File in Japan (Methyldopa Alphapharm Brand JDMF) empowers Methyldopa Alphapharm Brand 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 Alphapharm Brand JDMF during the approval evaluation for pharmaceutical products. At the time of Methyldopa Alphapharm Brand 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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