01 1Juzen Chemical Co., Ltd.
02 1Sanyo Chemical Research Institute Co., Ltd.
01 2Trimetoquinol Nord hydrochloride hydrate
01 1Gabon
02 1Japan
Trimetoquinol hydrochloride hydrate
Registration Number : 219MF10318
Registrant's Address : 1-10 Kibacho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2007-10-24
Trimetoquinol hydrochloride hydrate
Registration Number : 219MF10241
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
A Trimetoquinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimetoquinol, including repackagers and relabelers. The FDA regulates Trimetoquinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimetoquinol 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 Trimetoquinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimetoquinol supplier is an individual or a company that provides Trimetoquinol active pharmaceutical ingredient (API) or Trimetoquinol finished formulations upon request. The Trimetoquinol suppliers may include Trimetoquinol API manufacturers, exporters, distributors and traders.
click here to find a list of Trimetoquinol 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 Trimetoquinol Drug Master File in Japan (Trimetoquinol JDMF) empowers Trimetoquinol 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 Trimetoquinol JDMF during the approval evaluation for pharmaceutical products. At the time of Trimetoquinol 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 Trimetoquinol suppliers with JDMF on PharmaCompass.
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