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