01 1Katsura Chemical Co., Ltd.
02 1NARD Chemicals Inc.
03 1Sekisui Medical Co., Ltd.
01 1Timiperone
02 1Timiperone "first"
03 1Timiperone (production only)
01 3Japan
Registration Number : 218MF10272
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2006-02-17
Chimiperon (for manufacturing only)
Registration Number : 218MF10390
Registrant's Address : 2-6-1 Nishinagasucho, Amagasaki City, Hyogo Prefecture
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2010-04-05
Registration Number : 217MF10773
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2010-02-25
A Timiperone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Timiperone, including repackagers and relabelers. The FDA regulates Timiperone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Timiperone 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 Timiperone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Timiperone supplier is an individual or a company that provides Timiperone active pharmaceutical ingredient (API) or Timiperone finished formulations upon request. The Timiperone suppliers may include Timiperone API manufacturers, exporters, distributors and traders.
click here to find a list of Timiperone 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 Timiperone Drug Master File in Japan (Timiperone JDMF) empowers Timiperone 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 Timiperone JDMF during the approval evaluation for pharmaceutical products. At the time of Timiperone 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 Timiperone suppliers with JDMF on PharmaCompass.
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