Pfizer Inc. recalls Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of Pfize…

Recall date

September 24, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0161-2016

FDA classification

Class II

Brand / firm

Pfizer Inc.

Sold / distributed

Nationwide

Why it was recalled

Subpotent Drug

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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