01 1Kongo Chemical Co., Ltd.
01 1Nitric acid Bisuchiamin (production only)
01 1Japan
Bistiamine nitrate (for manufacturing purposes 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
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PharmaCompass offers a list of Nitric Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Nitric Acid manufacturer or Nitric Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Nitric Acid API Price utilized in the formulation of products. Nitric Acid API Price is not always fixed or binding as the Nitric Acid Price is obtained through a variety of data sources. The Nitric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aqua fortis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aqua fortis, including repackagers and relabelers. The FDA regulates Aqua fortis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aqua fortis API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Aqua fortis supplier is an individual or a company that provides Aqua fortis active pharmaceutical ingredient (API) or Aqua fortis finished formulations upon request. The Aqua fortis suppliers may include Aqua fortis API manufacturers, exporters, distributors and traders.
click here to find a list of Aqua fortis 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 Aqua fortis Drug Master File in Japan (Aqua fortis JDMF) empowers Aqua fortis 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 Aqua fortis JDMF during the approval evaluation for pharmaceutical products. At the time of Aqua fortis JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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