01 1Tateyama Chemical Co., Ltd.
02 1Zhejiang Apeloa Jiayuan Pharmaceutical Co. , Ltd.
01 1Bazedoxifene Acetate Chemexpress
02 1Bazedoxifene acetate
01 1China
02 1Japan
Bazedoxifene acetate "Tateyama"
Registration Number : 231MF10047
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2019-02-15
Latest Date of Registration : 2019-02-15
Bazedoxifene Acetate Chemexpress
Registration Number : 302MF10051
Registrant's Address : Hengdian Industry Zone, Dongyang, Zhejiang 322118 China
Initial Date of Registration : 2020-05-12
Latest Date of Registration : 2023-08-09
A Bazedoxifene Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bazedoxifene Acetate, including repackagers and relabelers. The FDA regulates Bazedoxifene Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bazedoxifene Acetate 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 Bazedoxifene Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bazedoxifene Acetate supplier is an individual or a company that provides Bazedoxifene Acetate active pharmaceutical ingredient (API) or Bazedoxifene Acetate finished formulations upon request. The Bazedoxifene Acetate suppliers may include Bazedoxifene Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Bazedoxifene Acetate 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 Bazedoxifene Acetate Drug Master File in Japan (Bazedoxifene Acetate JDMF) empowers Bazedoxifene Acetate 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 Bazedoxifene Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Bazedoxifene Acetate 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 Bazedoxifene Acetate suppliers with JDMF on PharmaCompass.
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