01 1Alembic Pharmaceuticals Limited
02 1Cheer Fine Pharmaceutical Co. , Ltd.
03 1Polaris AI Pharma Corp.
01 3Apixaban
01 1China
02 1India
03 1South 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 : 306MF10141
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2024-11-13
Latest Date of Registration : 2024-11-13
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PharmaCompass offers a list of Apixaban API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Apixaban manufacturer or Apixaban supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Apixaban manufacturer or Apixaban supplier.
PharmaCompass also assists you with knowing the Apixaban API Price utilized in the formulation of products. Apixaban API Price is not always fixed or binding as the Apixaban Price is obtained through a variety of data sources. The Apixaban Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A cc-395 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cc-395, including repackagers and relabelers. The FDA regulates cc-395 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cc-395 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 cc-395 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A cc-395 supplier is an individual or a company that provides cc-395 active pharmaceutical ingredient (API) or cc-395 finished formulations upon request. The cc-395 suppliers may include cc-395 API manufacturers, exporters, distributors and traders.
click here to find a list of cc-395 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 cc-395 Drug Master File in Japan (cc-395 JDMF) empowers cc-395 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 cc-395 JDMF during the approval evaluation for pharmaceutical products. At the time of cc-395 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 cc-395 suppliers with JDMF on PharmaCompass.
We have 3 companies offering cc-395
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