01 1Chemiclea Co., Ltd.
02 1DSM Nutritional Products Ltd.
03 2Nissin Pharma Co., Ltd.
01 1Japanese Pharmacopoeia menatetrenone (production only)
02 1Phytonadione
03 1Phytonadione Phytonadione / Vitamin K1
04 1Vitamin K150% dispersion "Nissin"
01 3Japan
02 1Netherlands
Japanese Pharmacopoeia Menatetrenone (for manufacturing purposes only)
Registration Number : 217MF11147
Registrant's Address : Quattro Muromachi Building 9F, 4-1-6 Muromachi, Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2006-12-18
Registration Number : 217MF11107
Registrant's Address : 1-25 Kanda Nishikicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2009-07-30
Registration Number : 217MF11106
Registrant's Address : 1-25 Kanda Nishikicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2009-05-13
Registration Number : 218MF10101
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2006-12-27
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PharmaCompass offers a list of Vitamin K1 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 K1 manufacturer or Vitamin K1 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin K1 manufacturer or Vitamin K1 supplier.
PharmaCompass also assists you with knowing the Vitamin K1 API Price utilized in the formulation of products. Vitamin K1 API Price is not always fixed or binding as the Vitamin K1 Price is obtained through a variety of data sources. The Vitamin K1 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fitomenadiona manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fitomenadiona, including repackagers and relabelers. The FDA regulates Fitomenadiona manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fitomenadiona 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 Fitomenadiona manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fitomenadiona supplier is an individual or a company that provides Fitomenadiona active pharmaceutical ingredient (API) or Fitomenadiona finished formulations upon request. The Fitomenadiona suppliers may include Fitomenadiona API manufacturers, exporters, distributors and traders.
click here to find a list of Fitomenadiona 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 Fitomenadiona Drug Master File in Japan (Fitomenadiona JDMF) empowers Fitomenadiona 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 Fitomenadiona JDMF during the approval evaluation for pharmaceutical products. At the time of Fitomenadiona 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 Fitomenadiona suppliers with JDMF on PharmaCompass.
We have 3 companies offering Fitomenadiona
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