01 2Muromachi Chemical Co., Ltd.
02 1Sanwa Chemical Co., Ltd.
03 1Sanyo Fine Co., Ltd.
01 1Japanese Pharmacopoeia warfarin potassium (production only)
02 1Warfarin Potassium (for manufacturing only)
03 1Warfarin potassium
04 1Warfarin potassium (production only)
01 1Gabon
02 3Japan
Warfarin Potassium (for manufacturing only)
Registration Number : 302MF10001
Registrant's Address : 1-38-5 Shinshotachicho, Omuta City, Fukuoka Prefecture
Initial Date of Registration : 2020-01-07
Latest Date of Registration : 2024-09-25
Warfarin Potassium (for manufacturing only)
Registration Number : 217MF10571
Registrant's Address : 1-38-5 Shinshotachicho, Omuta City, Fukuoka Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2008-03-28
Japanese Pharmacopoeia Warfarin Potassium (for manufacturing purposes only)
Registration Number : 218MF10554
Registrant's Address : 24-8 Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2020-03-23
Registration Number : 224MF10236
Registrant's Address : Osaka Prefecture, Osaka City, Nishi Ward, Awaza 1-12-18
Initial Date of Registration : 2012-12-20
Latest Date of Registration : 2012-12-20
A Potassium Warfarin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potassium Warfarin, including repackagers and relabelers. The FDA regulates Potassium Warfarin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potassium Warfarin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Potassium Warfarin supplier is an individual or a company that provides Potassium Warfarin active pharmaceutical ingredient (API) or Potassium Warfarin finished formulations upon request. The Potassium Warfarin suppliers may include Potassium Warfarin API manufacturers, exporters, distributors and traders.
click here to find a list of Potassium Warfarin 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 Potassium Warfarin Drug Master File in Japan (Potassium Warfarin JDMF) empowers Potassium Warfarin 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 Potassium Warfarin JDMF during the approval evaluation for pharmaceutical products. At the time of Potassium Warfarin 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 Potassium Warfarin suppliers with JDMF on PharmaCompass.
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