FDA recall D-0401-2015
AVKARE Inc. · Class III · drug
Product
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
Reason for recall
Subpotent Drug
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2015-02-27
- Report date
- 2015-03-11
- Termination date
- 2015-09-22
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Pulaski, TN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0401-2015