FDA recall D-0161-2016
Pfizer Inc. · Class II · drug
Product
Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of Pfizer Inc, NY, NY 10017, NDC 0009-0029-01
Reason for recall
Subpotent Drug
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2015-09-24
- Report date
- 2015-11-04
- Termination date
- 2017-05-08
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- New York, NY, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0161-2016