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

U.S. FDA Requirements: Moexipril Hydrochloride

Pharmaceutical / Drug Definition : Inhibits conversion of angiotensin I to the vasoconstrictor angiotensin II, inactivates bradykinin and other vasodilatory prostaglandins, increases plasma renin levels, and reduces aldosterone levels. Net effect is systemic vasodilation.

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

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


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