01 1Boryung Pharmaceutical Co. , Ltd.
02 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
03 1Hamari PFST Co., Ltd.
04 3Hamari Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Tamsulosin Hydrochloride
02 1Japanese Pharmacopoeia Tamsulosin hydrochloride
03 1Japanese Pharmacopoeia tamsulosin hydrochloride
04 2Tamsulosin hydrochloride
05 1Tamsulosin hydrochloride
01 4Japan
02 2South Korea
Registration Number : 226MF10100
Registrant's Address : 136, Changgyeonggung-ro, Jongno-gu, Seoul, Korea
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2014-05-14
Registration Number : 230MF10019
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Manse-gu, Hwaseong-si, Gyeonggi-do, Republic of...
Initial Date of Registration : 2018-02-05
Latest Date of Registration : 2018-02-05
Japanese Pharmacopoeia Tamsulosin Hydrochloride
Registration Number : 222MF10174
Registrant's Address : 1-4-29 Shibajima, Higashiyodogawa-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2010-06-18
Latest Date of Registration : 2010-06-18
Tamsulosin hydrochloride "Hamari"
Registration Number : 217MF11145
Registrant's Address : 1-4-29 Shibajima, Higashiyodogawa-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2006-09-22
Japanese Pharmacopoeia Tamsulosin Hydrochloride "Hamari"
Registration Number : 219MF10139
Registrant's Address : 1-4-29 Shibajima, Higashiyodogawa-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2007-04-18
Latest Date of Registration : 2007-04-18
Japanese Pharmacopoeia Tamsulosin Hydrochloride
Registration Number : 230MF10156
Registrant's Address : 1-19-40 Minamiko-Kita, Suminoe-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2018-11-14
Latest Date of Registration : 2022-05-25
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Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tamsulosin manufacturer or Tamsulosin supplier.
A Bio-0146 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bio-0146, including repackagers and relabelers. The FDA regulates Bio-0146 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bio-0146 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 Bio-0146 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Bio-0146 supplier is an individual or a company that provides Bio-0146 active pharmaceutical ingredient (API) or Bio-0146 finished formulations upon request. The Bio-0146 suppliers may include Bio-0146 API manufacturers, exporters, distributors and traders.
click here to find a list of Bio-0146 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 Bio-0146 Drug Master File in Japan (Bio-0146 JDMF) empowers Bio-0146 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 Bio-0146 JDMF during the approval evaluation for pharmaceutical products. At the time of Bio-0146 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 Bio-0146 suppliers with JDMF on PharmaCompass.
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