FDAFDA · Food and drugs·Recall number D-007-2013
Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,
Published October 17, 2012 · Recall initiated: October 3, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Paddock Laboratories, LLC
- Distributor
- Nationwide
- Lot
- 2012028142 exp. 1/2014
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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