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

U.S. FDA Requirements: Chlorpromazine Hydrochloride

Pharmaceutical / Drug Definition : May block postsynaptic dopamine receptors in brain and depress areas involved in wakefulness and emesis. Also possesses anticholinergic, antihistaminic, and adrenergic-blocking properties.

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

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


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