Registrar Corp Registrar Corp LinkedIn Registrar Corp Twitter Registrar Corp Facebook Registrar Corp Google+ Registrar Corp Youtube Channel Registrar Corp FDA News Blog
HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Dimenhydrinate

U.S. FDA Requirements: Dimenhydrinate

Pharmaceutical / Drug Definition : Prevents nausea and vomiting by inhibiting vestibular stimulation of chemoreceptor trigger zone and inhibiting stimulation of vomiting center in brain

In the United States, Dimenhydrinate is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Dimenhydrinate.

Registrar Corp assists Dimenhydrinate companies with:

  • FDA Registration Dimenhydrinate
  • FDA Listing Dimenhydrinate
  • FDA Label Requirements and Exceptions Dimenhydrinate
  • FDA Import Information Dimenhydrinate
  • FDA Detentions Dimenhydrinate (Dimenhydrinate Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Dimenhydrinate (Dimenhydrinate Suppliers)
       - Processors Dimenhydrinate
       - Repackers Dimenhydrinate
       - Relabelers Dimenhydrinate
       - Exporters Dimenhydrinate
       - Importers Dimenhydrinate
For more information about Dimenhydrinate, simply click below:

Live Help

U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2017 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco