Reported Jan 13, 2016 · Terminated
Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count bottles, Packaged by: PD-RX…
PD-Rx Pharmaceuticals, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PD-Rx Pharmaceuticals, Inc. · 727 N Ann Arbor Ave · Oklahoma City, OK · 73127-5822
Is this the product you have?
- Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count bottles
- Packaged byPD-RX Pharmaceuticals, Inc., Oklahoma City, OK, 73127
- MfgWockhardt Ltd., Mumbai, India
- NDC
a) 55289-964-02b) 55289-964-04
- Lot codes and dates
Lot #s: a) J12A48Exp 10/14L12A23Exp 12/14A13G04A13H14Exp 01/15B13E97Exp 02/15C13B55Exp 03/15J13F75L13C93A14F78A14H17B14A6Exp 08/15I13D47I13G28Exp 09/15J13D73J13D93 Exp 10/15K13E1811/15A14H06C14A49C14D01Exp 12/15A14B95 01/16
- Amount recalled
- 45,022 bottles
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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