01 2DDP Specialty Electronic Materials US 9, LLC
01 1LiveoTM Q7-9120 Silicone Fluid, 100 cSt
02 1LiveoTM Q7-9120 Silicone Fluid, 350 cSt
01 2U.S.A
LiveoT.M. Q7-9120 Silicone Fluid, 100 cSt
Registration Number : 303MF10091
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2021-06-07
Latest Date of Registration : 2021-06-07
LiveoT.M. Q7-9120 Silicone Fluid, 350 cSt
Registration Number : 303MF10087
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2021-06-03
Latest Date of Registration : 2021-06-03
A Dimethicone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimethicone, including repackagers and relabelers. The FDA regulates Dimethicone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimethicone 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 Dimethicone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dimethicone supplier is an individual or a company that provides Dimethicone active pharmaceutical ingredient (API) or Dimethicone finished formulations upon request. The Dimethicone suppliers may include Dimethicone API manufacturers, exporters, distributors and traders.
click here to find a list of Dimethicone 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 Dimethicone Drug Master File in Japan (Dimethicone JDMF) empowers Dimethicone 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 Dimethicone JDMF during the approval evaluation for pharmaceutical products. At the time of Dimethicone 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 Dimethicone suppliers with JDMF on PharmaCompass.
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