01 1Kongo Chemical Co., Ltd.
01 1Nitric acid Bisuchiamin (production only)
01 1Japan
Bisthioamine nitrate (for manufacturing only)
Registration Number : 217MF11210
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-03-09
A Nitric Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nitric Acid, including repackagers and relabelers. The FDA regulates Nitric Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nitric Acid 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 Nitric Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nitric Acid supplier is an individual or a company that provides Nitric Acid active pharmaceutical ingredient (API) or Nitric Acid finished formulations upon request. The Nitric Acid suppliers may include Nitric Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Nitric Acid 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 Nitric Acid Drug Master File in Japan (Nitric Acid JDMF) empowers Nitric Acid 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 Nitric Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Nitric Acid 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 Nitric Acid suppliers with JDMF on PharmaCompass.
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