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

U.S. FDA Requirements: Triamterene

Pharmaceutical / Drug Definition : Depresses sodium resorption and potassium excretion in renal distal tubule

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

Registrar Corp assists Triamterene companies with:

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