Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Limited
02 1DSM Nutritional Products France SAS
03 1DSM Nutritional Products Ltd.
04 1Minsheng Group Shaoxing Pharmaceutical Co. , Ltd.
05 1SperaNexus Co., Ltd.
01 1Japanese Pharmacopoeia riboflavin phosphate ester sodium
02 1Japanese Pharmacopoeia riboflavin phosphate ester sodium (manufactured only)
03 1Riboflavin 5'-Phosphate
04 1Riboflavin phosphate sodium
05 1Sodium riboflavin phosphate Riboflavin-5'-Phosphate Sodium
01 1China
02 1India
03 1Japan
04 2Netherlands
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registration Number : 306MF10052
Registrant's Address : 207/208, Udyog Bhavan, Sonawala Road, Goregaon East, Mumbai, India
Initial Date of Registration : 2024-04-03
Latest Date of Registration : 2024-04-03
Registration Number : 217MF10034
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2007-07-17
Japanese Pharmacopoeia Riboflavin Sodium Phosphate (For manufacturing purposes only)
Registration Number : 226MF10221
Registrant's Address : 315, Tanggong Road, Paojiang Industrial Zone, Shaoxing, P. R. China
Initial Date of Registration : 2014-11-17
Latest Date of Registration : 2014-11-17
Japanese Pharmacopoeia Riboflavin Sodium Phosphate
Registration Number : 219MF10120
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Riboflavin-5'-Phosphate Sodium
Registration Number : 217MF11123
Registrant's Address : 1 boulevard d'Alsace, F-68128 Village-Neuf, France
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2006-07-20
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PharmaCompass offers a list of Riboflavin 5 Phosphate Sodium 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 5 Phosphate Sodium manufacturer or Riboflavin 5 Phosphate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Riboflavin 5 Phosphate Sodium API Price utilized in the formulation of products. Riboflavin 5 Phosphate Sodium API Price is not always fixed or binding as the Riboflavin 5 Phosphate Sodium Price is obtained through a variety of data sources. The Riboflavin 5 Phosphate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hyryl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyryl, including repackagers and relabelers. The FDA regulates Hyryl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyryl 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 Hyryl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hyryl supplier is an individual or a company that provides Hyryl active pharmaceutical ingredient (API) or Hyryl finished formulations upon request. The Hyryl suppliers may include Hyryl API manufacturers, exporters, distributors and traders.
click here to find a list of Hyryl 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 Hyryl Drug Master File in Japan (Hyryl JDMF) empowers Hyryl 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 Hyryl JDMF during the approval evaluation for pharmaceutical products. At the time of Hyryl 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 Hyryl suppliers with JDMF on PharmaCompass.
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