01 1Active Pharma Inc.
02 1Daito Co., Ltd.
03 1Kyongbo Pharmaceutical Co. , Ltd.
04 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
05 1Tianish Laboratories Private Limited
06 1Yoshindo Co., Ltd.
01 5Blonanserin
02 1Blonanserin production dedicated
01 4Japan
02 1South Korea
03 1U.S.A
Registration Number : 229MF10182
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2017-10-03
Latest Date of Registration : 2021-03-09
Registration Number : 229MF10212
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2017-12-01
Latest Date of Registration : 2017-12-01
Blonanserin For manufacturing purposes only
Registration Number : 230MF10035
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2018-02-26
Latest Date of Registration : 2018-02-26
Registration Number : 229MF10221
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2017-12-18
Latest Date of Registration : 2021-06-18
Registration Number : 229MF10210
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2017-12-01
Latest Date of Registration : 2017-12-01
Registration Number : 230MF10005
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2018-01-10
Latest Date of Registration : 2018-01-10
A Blonanserin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Blonanserin, including repackagers and relabelers. The FDA regulates Blonanserin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Blonanserin 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 Blonanserin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Blonanserin supplier is an individual or a company that provides Blonanserin active pharmaceutical ingredient (API) or Blonanserin finished formulations upon request. The Blonanserin suppliers may include Blonanserin API manufacturers, exporters, distributors and traders.
click here to find a list of Blonanserin 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 Blonanserin Drug Master File in Japan (Blonanserin JDMF) empowers Blonanserin 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 Blonanserin JDMF during the approval evaluation for pharmaceutical products. At the time of Blonanserin 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 Blonanserin suppliers with JDMF on PharmaCompass.
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