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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.

In the United States, Moexipril Hydrochloride is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Moexipril Hydrochloride.

Registrar Corp assists Moexipril Hydrochloride companies with:

  • FDA Registration Moexipril Hydrochloride
  • FDA Listing Moexipril Hydrochloride
  • FDA Label Requirements and Exceptions Moexipril Hydrochloride
  • FDA Import Information Moexipril Hydrochloride
  • 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
For more information about Moexipril Hydrochloride, simply click below:

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U.S. FDA Regulations:

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

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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