01 1MENADIONA, S. L.
02 1NAKODA CHEMICALS LIMITED
03 1Nisshin Pharma Co., Ltd.
04 1Sanyo Fine Co., Ltd.
01 1Japanese Pharmacopoeia menatetrenone (production only)
02 3Menatetrenone
01 1Gabon
02 1India
03 1Japan
04 1Spain
Registration Number : 218MF10262
Registrant's Address : Poligono Inds. Mas Puigvert Ctra. National II, Km. 680,5,08389 Palafolls, Barcelona, ...
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2019-02-26
Registration Number : 218MF10404
Registrant's Address : Plot No. 64/A & 65/B, Phase-I, IDA, Jeedimetla, Hyderabad-500 055, Telangana State, I...
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2007-01-10
Registration Number : 217MF11114
Registrant's Address : 25 Kanda Nishikicho 1-chome, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2007-08-01
Japanese Pharmacopoeia Menatetrenone (for manufacturing only)
Registration Number : 226MF10065
Registrant's Address : Osaka Prefecture, Osaka City, Nishi Ward, Awaza 1-12-18
Initial Date of Registration : 2014-03-11
Latest Date of Registration : 2023-12-19
A Vitamin K2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin K2, including repackagers and relabelers. The FDA regulates Vitamin K2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin K2 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 Vitamin K2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vitamin K2 supplier is an individual or a company that provides Vitamin K2 active pharmaceutical ingredient (API) or Vitamin K2 finished formulations upon request. The Vitamin K2 suppliers may include Vitamin K2 API manufacturers, exporters, distributors and traders.
click here to find a list of Vitamin K2 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 Vitamin K2 Drug Master File in Japan (Vitamin K2 JDMF) empowers Vitamin K2 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 Vitamin K2 JDMF during the approval evaluation for pharmaceutical products. At the time of Vitamin K2 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 Vitamin K2 suppliers with JDMF on PharmaCompass.
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