EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 1Everlight Chemical Industrial Corporation
03 1Kyowa Pharma Chemical Co., Ltd.
04 1Piramal Healthcare (Canada) Limited
05 1Shanghai Tianwei Biopharmaceutical Co., Ltd.
06 1YS Life Science Co. ,Ltd
01 4Bimatoprost
02 1Bimatoprost "production-only"
03 1Bimatoprost (production only)
01 1China
02 1France
03 1India
04 1Japan
05 1South Korea
06 1Taiwan
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 229MF10098
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2017-05-24
Latest Date of Registration : 2017-05-24
Registration Number : 228MF10186
Registrant's Address : 6Floor, Chung Ting Building No. 77, Section 2, Tun Hua South Road, Taipei, Taiwan
Initial Date of Registration : 2016-09-20
Latest Date of Registration : 2017-07-24
Bimatoprost (for manufacturing purposes only)
Registration Number : 224MF10081
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2012-04-13
Latest Date of Registration : 2023-02-08
Registration Number : 220MF10035
Registrant's Address : 110 Industrial Parkway North, Aurora, Ontario L4G 3H4 Canada
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2009-12-22
Registration Number : 229MF10165
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2017-08-22
Latest Date of Registration : 2017-08-22
Bimatoprost "For manufacturing purposes only"
Registration Number : 229MF10152
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2017-08-04
Latest Date of Registration : 2017-08-04
A Bimatoprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bimatoprost, including repackagers and relabelers. The FDA regulates Bimatoprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bimatoprost 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 Bimatoprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bimatoprost supplier is an individual or a company that provides Bimatoprost active pharmaceutical ingredient (API) or Bimatoprost finished formulations upon request. The Bimatoprost suppliers may include Bimatoprost API manufacturers, exporters, distributors and traders.
click here to find a list of Bimatoprost 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 Bimatoprost Drug Master File in Japan (Bimatoprost JDMF) empowers Bimatoprost 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 Bimatoprost JDMF during the approval evaluation for pharmaceutical products. At the time of Bimatoprost 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 Bimatoprost suppliers with JDMF on PharmaCompass.
We have 6 companies offering Bimatoprost
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