Univasc

Active Ingredient(s): Moexipril
FDA Approved: * April 19, 1995
Pharm Company: * SCHWARZ PHARMA
Category: Blood Pressure

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Univasc Overview

Moexipril hydrochloride is a potent orally active nonsulfhydryl angiotensin converting enzyme inhibitor (ACE inhibitor)[1] which is used for the treatment of hypertension and congestive heart failure. Moexipril can be administered alone or with other antihypertensives or diuretics.[2] It works by inhibiting the conversion of angiotensin I to angiotensin II.[3] Moexipril is available from Schwarz Pharma under the trade name Univasc.[3&...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Moexipril

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Possible Dosages for this and Related Drugs:

Moexipril
  • Tablet: 15mg, 7.5mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Univasc: (2 results)

Sorted by National Drug Code
  • 0091-3707 Univasc 7.5 mg Oral Tablet by Ucb, Inc.
  • 0091-3715 Univasc 15 mg Oral Tablet by Ucb, Inc.

Other drugs which contain Moexipril or a similar ingredient: (3 results)






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