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: Celecoxib

U.S. FDA Requirements: Celecoxib

Pharmaceutical / Drug Definition : Exhibits anti-inflammatory, analgesic, and antipyretic action due to inhibition of COX-2 enzyme

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

Registrar Corp assists Celecoxib companies with:

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