01 2BASF Company Ltd
02 1DSM Nutritional Products Ltd.
03 1Kyowa Pharma Chemical Co., Ltd.
01 1Japanese Pharmacopoeia riboflavin butyric acid ester (production only)
02 1Riboflavin
03 1Riboflavin Riboflavin
04 1Riboflavin Riboflavin Universal
01 2Germany
02 1Japan
03 1Netherlands
Registration Number : 228MF10235
Registrant's Address : 14-16F KCCI Bldg. , 39, Sejongdaero, Jung-gu, Seoul, Republic of Korea
Initial Date of Registration : 2016-12-26
Latest Date of Registration : 2016-12-26
Registration Number : 217MF10986
Registrant's Address : 14-16F KCCI Bldg. , 39, Sejongdaero, Jung-gu, Seoul, Republic of Korea
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2010-06-04
Japanese Pharmacopoeia Riboflavin Butyrate (for manufacturing only)
Registration Number : 221MF10100
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2009-05-27
Registration Number : 217MF11283
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-07-20
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PharmaCompass offers a list of Riboflavin 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 Riboflavin manufacturer or Riboflavin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Riboflavin manufacturer or Riboflavin supplier.
PharmaCompass also assists you with knowing the Riboflavin API Price utilized in the formulation of products. Riboflavin API Price is not always fixed or binding as the Riboflavin Price is obtained through a variety of data sources. The Riboflavin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aqua-Flave manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aqua-Flave, including repackagers and relabelers. The FDA regulates Aqua-Flave manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aqua-Flave 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 Aqua-Flave manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aqua-Flave supplier is an individual or a company that provides Aqua-Flave active pharmaceutical ingredient (API) or Aqua-Flave finished formulations upon request. The Aqua-Flave suppliers may include Aqua-Flave API manufacturers, exporters, distributors and traders.
click here to find a list of Aqua-Flave 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 Aqua-Flave Drug Master File in Japan (Aqua-Flave JDMF) empowers Aqua-Flave 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 Aqua-Flave JDMF during the approval evaluation for pharmaceutical products. At the time of Aqua-Flave 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 Aqua-Flave suppliers with JDMF on PharmaCompass.
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