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