01 1Fushimi Pharmaceutical Co., Ltd.
01 1Homo sulfamine (for manufacturing only)
01 1Japan
Homosulfamine (for manufacturing only)
Registration Number : 231MF10085
Registrant's Address : 1676 Nakatsucho, Marugame City, Kagawa Prefecture
Initial Date of Registration : 2019-04-09
Latest Date of Registration : 2019-04-09
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PharmaCompass offers a list of Sulfanilamide 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 Sulfanilamide manufacturer or Sulfanilamide supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfanilamide API Price utilized in the formulation of products. Sulfanilamide API Price is not always fixed or binding as the Sulfanilamide Price is obtained through a variety of data sources. The Sulfanilamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sulfana manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfana, including repackagers and relabelers. The FDA regulates Sulfana manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfana 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 Sulfana manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulfana supplier is an individual or a company that provides Sulfana active pharmaceutical ingredient (API) or Sulfana finished formulations upon request. The Sulfana suppliers may include Sulfana API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfana 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 Sulfana Drug Master File in Japan (Sulfana JDMF) empowers Sulfana 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 Sulfana JDMF during the approval evaluation for pharmaceutical products. At the time of Sulfana 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 Sulfana suppliers with JDMF on PharmaCompass.
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