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 : Le'anjiang 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 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
A Thiamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiamine Hydrochloride, including repackagers and relabelers. The FDA regulates Thiamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiamine Hydrochloride 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 Thiamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thiamine Hydrochloride supplier is an individual or a company that provides Thiamine Hydrochloride active pharmaceutical ingredient (API) or Thiamine Hydrochloride finished formulations upon request. The Thiamine Hydrochloride suppliers may include Thiamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Thiamine Hydrochloride 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 Hydrochloride Drug Master File in Japan (Thiamine Hydrochloride JDMF) empowers Thiamine Hydrochloride 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 Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Thiamine Hydrochloride 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 Thiamine Hydrochloride suppliers with JDMF on PharmaCompass.
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