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

U.S. FDA Requirements: Cetirizine Hydrochloride

Pharmaceutical / Drug Definition : Antagonizes histamine's effects at histamine1-receptor sites, preventing allergic response. Also has mild bronchodilatory effects and blocks histamine-induced bronchoconstriction in asthma.

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

Registrar Corp assists Cetirizine Hydrochloride companies with:

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