01 1Kyorin Pharmaceutical Group Factory Co., Ltd.
02 1Ryoto Fine Co., Ltd.
03 1Sanyo Chemical Research Institute Co., Ltd.
04 1Yoshindo Co., Ltd.
01 4Imidafenacin
01 1Gabon
02 3Japan
Registration Number : 219MF10220
Registrant's Address : 1-3-7 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
Registration Number : 231MF10015
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2019-01-23
Latest Date of Registration : 2022-04-06
Registration Number : 230MF10145
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2018-10-23
Latest Date of Registration : 2018-10-23
Registration Number : 230MF10150
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2018-11-07
Latest Date of Registration : 2018-11-07
A Imidafenacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imidafenacin, including repackagers and relabelers. The FDA regulates Imidafenacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imidafenacin 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 Imidafenacin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imidafenacin supplier is an individual or a company that provides Imidafenacin active pharmaceutical ingredient (API) or Imidafenacin finished formulations upon request. The Imidafenacin suppliers may include Imidafenacin API manufacturers, exporters, distributors and traders.
click here to find a list of Imidafenacin 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 Imidafenacin Drug Master File in Japan (Imidafenacin JDMF) empowers Imidafenacin 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 Imidafenacin JDMF during the approval evaluation for pharmaceutical products. At the time of Imidafenacin 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 Imidafenacin suppliers with JDMF on PharmaCompass.
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