Reported Feb 23, 2022 · Terminated
Alprazolam Tablets, USP 1.0 mg, packaged in a) 100-count bottles (NDC 67253-902-10), b) 500-count bottles (NDC…
ANI 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: ANI Pharmaceuticals, Inc. · 210 W Main St · Baudette, MN · 56623-2467
Is this the product you have?
3 of 3 products
| # | Product as published |
|---|---|
| 1 | 100-count bottles (NDC 67253-902-10) |
| 2 | 500-count bottles (NDC 67253-902-50), and |
| 3 | 1000-count bottles (NDC 67253-902-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 |
- Lot codes and dates
3 of 3 products
Products covered by this recall # Product as published 1 19B081A, Exp. Date 02/2022; 19E088A, 19E089A, Exp. Date 05/2022 2 19A102B, Exp. Date 02/2022; 19D067B, 19D068B, Exp. Date 04/2022; 19D070C, Exp. Date 05/2022. 3 19F045C, 19F046C, Exp. Date 06/2022; 19B082C, 19B083C, Exp. Date 03/2022; 19D069C, Exp. Date 05/2022. - Amount recalled
- 173,499 bottles
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
cGMP Deviations
This product could cause temporary or reversible health problems — stop using it.
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