01 1DSM Nutritional Products GmbH
02 1DSM Nutritional Products Ltd.
03 1Jiangxi Tianxin Pharmaceutical Co. , Ltd.
04 1Tianjin Zhongjin Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia thiamine nitrification product
02 1Nitric acid thiamine Thiamine Mononitrate
03 1Thiamine nitrification product
04 1Thiamine nitrification product
01 2China
02 2Netherlands
Thiamine Nitrate "For Manufacturing Use Only"
Registration Number : 225MF10200
Registrant's Address : Le'anjiang Industrial Zone, Leping, Jiangxi, 333300, People's Republic of China
Initial Date of Registration : 2013-11-11
Latest Date of Registration : 2013-11-11
Registration Number : 217MF11285
Registrant's Address : Emil-Barell-Str. 3, D-79639 Grenzach-Wyhlen, Germany
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-09-22
Japanese Pharmacopoeia Thiamine Nitrate
Registration Number : 219MF10117
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Registration Number : 218MF10842
Registrant's Address : #17, Bridge, Weihuan xian, Jiefang South Road, Tianjin, People Republic of China
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2006-10-20
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PharmaCompass offers a list of Thiamine Mononitrate 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 Thiamine Mononitrate manufacturer or Thiamine Mononitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Thiamine Mononitrate API Price utilized in the formulation of products. Thiamine Mononitrate API Price is not always fixed or binding as the Thiamine Mononitrate Price is obtained through a variety of data sources. The Thiamine Mononitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard suppliers may include Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard 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 Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard Drug Master File in Japan (Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard JDMF) empowers Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard 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 Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard JDMF during the approval evaluation for pharmaceutical products. At the time of Thiamine nitrate, European Pharmacopoeia (EP) Reference Standard JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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