01 1Cytec Industries Inc.
01 1Outsider regulations dioctyl sodium sulfosuccinate (manufactured only)
01 1Belgium
Dioctyl Sodium Sulfosuccinate (for manufacturing only)
Registration Number : 218MF10083
Registrant's Address : 504 Carnegie Center, Princeton, NJ 08540, U.S. S. A.
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-03-19
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PharmaCompass offers a list of Docusate Sodium 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 Docusate Sodium manufacturer or Docusate Sodium supplier for your needs.
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A sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate, including repackagers and relabelers. The FDA regulates sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate 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 sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate supplier is an individual or a company that provides sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate active pharmaceutical ingredient (API) or sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate finished formulations upon request. The sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate suppliers may include sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate 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 sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate Drug Master File in Japan (sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate JDMF) empowers sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate 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 sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate JDMF during the approval evaluation for pharmaceutical products. At the time of sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate 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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We have 1 companies offering sodium 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate
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