Azurity Pharmaceuticals, Inc. recalls Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals,
Recalled February 7, 2024 · FDA recall D-0323-2024 · Azurity Pharmaceuticals
Hazard
Labeling: Label Mix-up · FDA Class I
Units
4,662 bottles
Sold at
USA nationwide
Description
Labeling: Label Mix-up
Product
Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Georgia, 30328, NDC 24338-856-03
Manufacturer(s)
Azurity Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →