01 1DSM Nutritional Products Ltd.
02 1Jiangxi Tianxin Pharmaceutical Co. , Ltd.
03 1Tianjin Zhongjin Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia thiamine nitrification product
02 1Thiamine nitrification product
03 1Thiamine nitrification product
01 2China
02 1Netherlands
Thiamine nitrate "For manufacturing purposes 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
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 Mononitrato de tiamina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mononitrato de tiamina, including repackagers and relabelers. The FDA regulates Mononitrato de tiamina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mononitrato de tiamina 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 Mononitrato de tiamina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mononitrato de tiamina supplier is an individual or a company that provides Mononitrato de tiamina active pharmaceutical ingredient (API) or Mononitrato de tiamina finished formulations upon request. The Mononitrato de tiamina suppliers may include Mononitrato de tiamina API manufacturers, exporters, distributors and traders.
click here to find a list of Mononitrato de tiamina 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 Mononitrato de tiamina Drug Master File in Japan (Mononitrato de tiamina JDMF) empowers Mononitrato de tiamina 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 Mononitrato de tiamina JDMF during the approval evaluation for pharmaceutical products. At the time of Mononitrato de tiamina 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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