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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.

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

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
For more information about Loratadine, 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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