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
100
PharmaCompass offers a list of Vitamin K2 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 Vitamin K2 manufacturer or Vitamin K2 supplier for your needs.
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PharmaCompass also assists you with knowing the Vitamin K2 API Price utilized in the formulation of products. Vitamin K2 API Price is not always fixed or binding as the Vitamin K2 Price is obtained through a variety of data sources. The Vitamin K2 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Menatetrenone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menatetrenone, including repackagers and relabelers. The FDA regulates Menatetrenone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menatetrenone 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 Menatetrenone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Menatetrenone supplier is an individual or a company that provides Menatetrenone active pharmaceutical ingredient (API) or Menatetrenone finished formulations upon request. The Menatetrenone suppliers may include Menatetrenone API manufacturers, exporters, distributors and traders.
click here to find a list of Menatetrenone 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 Menatetrenone Drug Master File in Japan (Menatetrenone JDMF) empowers Menatetrenone 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 Menatetrenone JDMF during the approval evaluation for pharmaceutical products. At the time of Menatetrenone 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 Menatetrenone suppliers with JDMF on PharmaCompass.
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