Quinapril Tablets USP, 40 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026869115, NDC 50268-691-15

FDA recall notice · announced March 11, 2015 · Avkare

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

Reason for recall

Subpotent Drug

Notes

Distribution: Nationwide
Lot/code information: Lot number: I1407932, Exp. 02/2016
Quantity: 431 unit dose packs
Status: Terminated
Products in this recall event:
- Quinapril Tablets USP, 5 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026868815, NDC 50268-688-15 (D-0401-2015)
- Quinapril Tablets USP, 40 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026869115, NDC 50268-691-15 (D-0402-2015)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.