01 1Cytec Industries Inc.
01 1Outsider regulations dioctyl sodium sulfosuccinate (manufactured only)
01 1Belgium
Dioctyl sodium sulfosuccinate (for manufacturing purposes 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
13
PharmaCompass offers a list of Docusate Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Docusate Sodium manufacturer or Docusate Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Docusate Sodium manufacturer or Docusate Sodium supplier.
A Manoxal OT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Manoxal OT, including repackagers and relabelers. The FDA regulates Manoxal OT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Manoxal OT 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 Manoxal OT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Manoxal OT supplier is an individual or a company that provides Manoxal OT active pharmaceutical ingredient (API) or Manoxal OT finished formulations upon request. The Manoxal OT suppliers may include Manoxal OT API manufacturers, exporters, distributors and traders.
click here to find a list of Manoxal OT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Manoxal OT Drug Master File in Japan (Manoxal OT JDMF) empowers Manoxal OT 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 Manoxal OT JDMF during the approval evaluation for pharmaceutical products. At the time of Manoxal OT 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 Manoxal OT suppliers with JDMF on PharmaCompass.
