01 1Sanwa Chemical Co., Ltd.
01 1p- guanidino benzoic acid hydrochloride
01 1Japan
p-Guanidinobenzoic acid hydrochloride
Registration Number : 225MF10136
Registrant's Address : 24-8 Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture
Initial Date of Registration : 2013-07-23
Latest Date of Registration : 2013-07-23
A Thiaproline-M-Amino Benzoic Acid Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiaproline-M-Amino Benzoic Acid Hydrochloride, including repackagers and relabelers. The FDA regulates Thiaproline-M-Amino Benzoic Acid Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiaproline-M-Amino Benzoic Acid 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.
A Thiaproline-M-Amino Benzoic Acid Hydrochloride supplier is an individual or a company that provides Thiaproline-M-Amino Benzoic Acid Hydrochloride active pharmaceutical ingredient (API) or Thiaproline-M-Amino Benzoic Acid Hydrochloride finished formulations upon request. The Thiaproline-M-Amino Benzoic Acid Hydrochloride suppliers may include Thiaproline-M-Amino Benzoic Acid Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Thiaproline-M-Amino Benzoic Acid 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 Thiaproline-M-Amino Benzoic Acid Hydrochloride Drug Master File in Japan (Thiaproline-M-Amino Benzoic Acid Hydrochloride JDMF) empowers Thiaproline-M-Amino Benzoic Acid 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 Thiaproline-M-Amino Benzoic Acid Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Thiaproline-M-Amino Benzoic Acid 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 Thiaproline-M-Amino Benzoic Acid Hydrochloride suppliers with JDMF on PharmaCompass.
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