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
Reported: November 4, 2015 Initiated: September 24, 2015 #D-0161-2016
Product Description
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
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 21,120 HDPE bottles
- Distribution
- Nationwide
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Pfizer Inc.. Units affected: 21,120 HDPE bottles.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 4, 2015. Severity: Moderate. Recall number: D-0161-2016.
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