01 1DSM Nutritional Products GmbH
02 1DSM Nutritional Products Ltd.
03 1Jiangxi Tianxin Pharmaceutical Co. , Ltd.
01 1Japanese Pharmacopoeia thiamine chloride hydrochloride salt
02 1Thiamine chloride hydrochloride "production-only"
03 1Thiamine hydrochloride Thiamine Hydrochloride
01 1China
02 2Netherlands
Thiamine chloride hydrochloride (for manufacturing purposes only)
Registration Number : 224MF10126
Registrant's Address : Leping Industrial Zone, Leping, Jiangxi, 333300, People's Republic of China
Initial Date of Registration : 2012-07-13
Latest Date of Registration : 2012-07-13
Japanese Pharmacopoeia Thiamine Chloride Hydrochloride
Registration Number : 219MF10116
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 : 217MF11284
Registrant's Address : Emil-Barell-Str. 3, D-79639 Grenzach-Wyhlen, Germany
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-07-20
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PharmaCompass offers a list of Thiamine Hydrochloride 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 Hydrochloride manufacturer or Thiamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thiamine Hydrochloride manufacturer or Thiamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Thiamine Hydrochloride API Price utilized in the formulation of products. Thiamine Hydrochloride API Price is not always fixed or binding as the Thiamine Hydrochloride Price is obtained through a variety of data sources. The Thiamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trophite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trophite, including repackagers and relabelers. The FDA regulates Trophite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trophite 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 Trophite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trophite supplier is an individual or a company that provides Trophite active pharmaceutical ingredient (API) or Trophite finished formulations upon request. The Trophite suppliers may include Trophite API manufacturers, exporters, distributors and traders.
click here to find a list of Trophite 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 Trophite Drug Master File in Japan (Trophite JDMF) empowers Trophite 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 Trophite JDMF during the approval evaluation for pharmaceutical products. At the time of Trophite 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 Trophite suppliers with JDMF on PharmaCompass.
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