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

U.S. FDA Requirements: Loratadine

Pharmaceutical / Drug Definition : Selective histamine1-receptor antagonist. Blocks peripheral effects of histamine release during allergic reactions, decreasing or preventing allergy symptoms.

Registrar Corp assists Loratadine companies with:

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

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


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