US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 29, 2015 (11 years ago)

Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP Deviations: This recall is a result of the original manufacturer's recall, in which the firm did not adequately investigate customer complaints.

What was recalled

Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count bottles, Packaged by: PD-RX Pharmaceuticals, Inc., Oklahoma City, OK, 73127, Mfg: Wockhardt Ltd., Mumbai, India, NDC: a) 55289-964-02, b) 55289-964-04.

Recalling firm
PD-Rx Pharmaceuticals, Inc.
Origin
OK, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0560-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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