EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 1Fermion Oy
03 1Boryung Pharmaceutical Co. , Ltd.
04 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
05 1Hamari PFST Co., Ltd.
06 3Hamari Pharmaceuticals Co., Ltd.
07 1Ohara Pharmaceutical Co., Ltd.
08 1Sanyo Chemical Research Institute Co., Ltd.
09 1YS Life Science Co. , Ltd.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 225MF10100
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2013-05-09
Latest Date of Registration : 2013-05-09
With Fermion, start the journey of your innovative API.
Registration Number : 219MF10365
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2021-05-27
A Tamsulosin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamsulosin HCl, including repackagers and relabelers. The FDA regulates Tamsulosin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamsulosin HCl 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 Tamsulosin HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tamsulosin HCl supplier is an individual or a company that provides Tamsulosin HCl active pharmaceutical ingredient (API) or Tamsulosin HCl finished formulations upon request. The Tamsulosin HCl suppliers may include Tamsulosin HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Tamsulosin HCl 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 Tamsulosin HCl Drug Master File in Japan (Tamsulosin HCl JDMF) empowers Tamsulosin HCl 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 Tamsulosin HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Tamsulosin HCl 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 Tamsulosin HCl suppliers with JDMF on PharmaCompass.
We have 8 companies offering Tamsulosin HCl
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