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 PABS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PABS, including repackagers and relabelers. The FDA regulates PABS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PABS 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 PABS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PABS supplier is an individual or a company that provides PABS active pharmaceutical ingredient (API) or PABS finished formulations upon request. The PABS suppliers may include PABS API manufacturers, exporters, distributors and traders.
click here to find a list of PABS 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 PABS Drug Master File in Japan (PABS JDMF) empowers PABS 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 PABS JDMF during the approval evaluation for pharmaceutical products. At the time of PABS 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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