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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Dapsone

U.S. FDA Requirements: Dapsone

Pharmaceutical / Drug Definition : Bactericidal and bacteriostatic against Mycobacterium leprae. Action in dermatitis herpetiformis not established.

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

Registrar Corp assists Dapsone companies with:

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

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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.
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