Is Moexipril recalled?

3 FDA recalls mention Moexipril. The most recent are listed below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Moexipril.

Class II · Moderate risk Terminated Dec 14, 2017

Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA…

Reason Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during…

Teva Pharmaceuticals USA NDC 0093-5213-01 D-0208-2018

Class II · Moderate risk Terminated Jul 24, 2015

univasc (moexipril HCl) tablets, 7.5 mg, 100 Ct Bottle, Rx Only. Manufactured for UCB, Inc., Smyrna, GA 30080. NDC: 0091-3707-01.

Reason Failed Dissolution Testing: Failed 24 month dissolution testing.

Ucb, Inc D-1348-2015

Class II · Moderate risk Terminated Oct 3, 2012

Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,

Reason Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril HCl Tablets 7.5mg (expiration 1/2014) because of a non-conformity…

Paddock Laboratories, LLC NDC 0574-0110-01 D-007-2013

Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA…

univasc (moexipril HCl) tablets, 7.5 mg, 100 Ct Bottle, Rx Only. Manufactured for UCB, Inc., Smyrna, GA 30080. NDC: 0091-3707-01.

Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,

Get an alert if your medication is recalled