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

U.S. FDA Requirements: Labetalol Hydrochloride

Pharmaceutical / Drug Definition : Blocks stimulation of beta1- and beta2-adrenergic receptor sites and alpha1-adrenergic receptors, decreasing myocardial contractile force and enhancing coronary artery blood flow and myocardial perfusion. Net effect is decreased heart rate and blood pressure.

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

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


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