01 1Alembic Pharmaceuticals Limited
02 1Cheer Fine Pharmaceutical Co. , Ltd.
03 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 1Polaris AI Pharma Corp.
05 1RUYUAN HEC PHARM CO. , LTD.
06 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
01 6Apixaban
01 3China
02 1India
03 2South Korea
Registration Number : 307MF10036
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2025-02-19
Latest Date of Registration : 2025-02-19
Registration Number : 307MF10097
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2025-08-06
Latest Date of Registration : 2025-08-06
Registration Number : 308MF10018
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2026-01-21
Latest Date of Registration : 2026-01-21
Registration Number : 308MF10036
Registrant's Address : Xiaba Development Zone, Ruyuan County, Shaoguan City, Guangdong Province, P. R. China
Initial Date of Registration : 2026-02-12
Latest Date of Registration : 2026-02-12
Registration Number : 306MF10141
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Manse-gu, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2024-11-13
Latest Date of Registration : 2024-11-13
Registration Number : 308MF10014
Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China
Initial Date of Registration : 2026-01-15
Latest Date of Registration : 2026-01-15
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A BMS 562247 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BMS 562247, including repackagers and relabelers. The FDA regulates BMS 562247 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BMS 562247 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BMS 562247 supplier is an individual or a company that provides BMS 562247 active pharmaceutical ingredient (API) or BMS 562247 finished formulations upon request. The BMS 562247 suppliers may include BMS 562247 API manufacturers, exporters, distributors and traders.
click here to find a list of BMS 562247 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 BMS 562247 Drug Master File in Japan (BMS 562247 JDMF) empowers BMS 562247 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 BMS 562247 JDMF during the approval evaluation for pharmaceutical products. At the time of BMS 562247 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 BMS 562247 suppliers with JDMF on PharmaCompass.
We have 6 companies offering BMS 562247
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