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

U.S. FDA Requirements: Hydroxyzine Pamoate

Pharmaceutical / Drug Definition : Anxiolytic and sedative effects may stem from suppression of activity in subcortical levels of CNS. Antihistamine effects may result from histamine suppression at cellular receptor sites.

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

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


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