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

U.S. FDA Requirements: Propranolol Hydrochloride

Pharmaceutical / Drug Definition : Blocks stimulation of beta1-adrenergic (myocardial) and beta2-adrenergic (pulmonary, vascular, and uterine) receptor sites. This action decreases cardiac output, slows heart rate, and reduces blood pressure.

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

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


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