01 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
02 1Fuji Chemical Industry Co., Ltd.
03 1Shiono Finesse Co., Ltd.
04 1UBE Co., Ltd.
05 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
01 3Silodosin
02 1Silodosin
03 1Silodosin (production only)
01 1China
02 3Japan
03 1South Korea
Registration Number : 230MF10008
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Manse-gu, Hwaseong-si, Gyeonggi-do, Republic of...
Initial Date of Registration : 2018-01-18
Latest Date of Registration : 2023-10-12
Silodosin (for manufacturing purposes only)
Registration Number : 229MF10126
Registrant's Address : 55 Yokohoonji, Kamiichi-machi, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 229MF10119
Registrant's Address : 3-1-6 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2017-07-10
Latest Date of Registration : 2017-07-10
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
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
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PharmaCompass offers a list of Silodosin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Silodosin manufacturer or Silodosin supplier for your needs.
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A Urorec manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urorec, including repackagers and relabelers. The FDA regulates Urorec manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urorec 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 Urorec manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Urorec supplier is an individual or a company that provides Urorec active pharmaceutical ingredient (API) or Urorec finished formulations upon request. The Urorec suppliers may include Urorec API manufacturers, exporters, distributors and traders.
click here to find a list of Urorec suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Urorec Drug Master File in Japan (Urorec JDMF) empowers Urorec 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 Urorec JDMF during the approval evaluation for pharmaceutical products. At the time of Urorec 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 Urorec suppliers with JDMF on PharmaCompass.
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