01 1Chengdu Easton Biopharmaceuticals Co. , Ltd.
02 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
03 1Fuji Chemical Industry Co., Ltd.
04 1Sanyo Chemical Research Institute Co., Ltd.
05 1Shiono Finesse Co., Ltd.
06 1UBE Inc.
07 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
01 5Silodosin
02 1Silodosin
03 1Silodosin (production only)
01 2China
02 1Gabon
03 3Japan
04 1South Korea
Registration Number : 230MF10008
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2018-01-18
Latest Date of Registration : 2023-10-12
Silodosin (for manufacturing only)
Registration Number : 229MF10126
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 229MF10119
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2017-07-10
Latest Date of Registration : 2017-07-10
Registration Number : 230MF10012
Registrant's Address : No. 8, Xiyuan Avenue, Hi-Tech District, Chengdu, 611731, China.
Initial Date of Registration : 2018-01-30
Latest Date of Registration : 2022-06-28
Registration Number : 230MF10002
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2018-01-10
Latest Date of Registration : 2018-01-10
Registration Number : 229MF10191
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2017-10-30
Latest Date of Registration : 2017-10-30
Silodosin "For manufacturing purposes only"
Registration Number : 230MF10036
Registrant's Address : Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang Province, People's Republ...
Initial Date of Registration : 2018-02-26
Latest Date of Registration : 2018-02-26
A Silodosin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Silodosin, including repackagers and relabelers. The FDA regulates Silodosin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Silodosin 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 Silodosin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Silodosin supplier is an individual or a company that provides Silodosin active pharmaceutical ingredient (API) or Silodosin finished formulations upon request. The Silodosin suppliers may include Silodosin API manufacturers, exporters, distributors and traders.
click here to find a list of Silodosin 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 Silodosin Drug Master File in Japan (Silodosin JDMF) empowers Silodosin 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 Silodosin JDMF during the approval evaluation for pharmaceutical products. At the time of Silodosin 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 Silodosin suppliers with JDMF on PharmaCompass.
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