01 1Fushimi Pharmaceutical Co., Ltd.
01 15 - (- 4-chlorobutyl) -1-cyclohexyl tetrazole
01 1Japan
5-(-4-chlorobutyl)-1-cyclohexyltetrazole
Registration Number : 219MF10217
Registrant's Address : 1676 Nakatsucho, Marugame City, Kagawa Prefecture
Initial Date of Registration : 2007-06-25
Latest Date of Registration : 2007-06-25
A 5-Cyclohexyl-2H-Tetrazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5-Cyclohexyl-2H-Tetrazole, including repackagers and relabelers. The FDA regulates 5-Cyclohexyl-2H-Tetrazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5-Cyclohexyl-2H-Tetrazole API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 5-Cyclohexyl-2H-Tetrazole supplier is an individual or a company that provides 5-Cyclohexyl-2H-Tetrazole active pharmaceutical ingredient (API) or 5-Cyclohexyl-2H-Tetrazole finished formulations upon request. The 5-Cyclohexyl-2H-Tetrazole suppliers may include 5-Cyclohexyl-2H-Tetrazole API manufacturers, exporters, distributors and traders.
click here to find a list of 5-Cyclohexyl-2H-Tetrazole 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 5-Cyclohexyl-2H-Tetrazole Drug Master File in Japan (5-Cyclohexyl-2H-Tetrazole JDMF) empowers 5-Cyclohexyl-2H-Tetrazole 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 5-Cyclohexyl-2H-Tetrazole JDMF during the approval evaluation for pharmaceutical products. At the time of 5-Cyclohexyl-2H-Tetrazole 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 5-Cyclohexyl-2H-Tetrazole suppliers with JDMF on PharmaCompass.
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