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Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427...

FDA Recall #D-007-2013 — Class II — October 3, 2012

Recall #D-007-2013 Date: October 3, 2012 Classification: Class II Status: Terminated

Product Description

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

Reason for Recall

Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril HCl Tablets 7.5mg (expiration 1/2014) because of a non-conformity dissolution failure result found during routine stability testing at the 6 month test interval.

Recalling Firm

Paddock Laboratories, LLC — Minneapolis, MN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

2267 bottles

Distribution

Nationwide

Code Information

2012028142 exp. 1/2014

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

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