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

U.S. FDA Requirements: Desloratadine

Pharmaceutical / Drug Definition : Suppresses histamine release at peripheral histamine1-receptor sites

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

Registrar Corp assists Desloratadine companies with:

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