01 1Fushimi Pharmaceutical Co., Ltd.
01 1Homo sulfamine (for manufacturing only)
01 1Japan
Homosulfamine (for manufacturing purposes 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 sulfanilamide sodium salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sulfanilamide sodium salt, including repackagers and relabelers. The FDA regulates sulfanilamide sodium salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sulfanilamide sodium salt 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 sulfanilamide sodium salt supplier is an individual or a company that provides sulfanilamide sodium salt active pharmaceutical ingredient (API) or sulfanilamide sodium salt finished formulations upon request. The sulfanilamide sodium salt suppliers may include sulfanilamide sodium salt API manufacturers, exporters, distributors and traders.
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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 sulfanilamide sodium salt Drug Master File in Japan (sulfanilamide sodium salt JDMF) empowers sulfanilamide sodium salt 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 sulfanilamide sodium salt JDMF during the approval evaluation for pharmaceutical products. At the time of sulfanilamide sodium salt 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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