Reported Jan 25, 2023 · Terminated
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle,…
Lannett Company Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Lannett Company Inc. · 1101 C Ave W · Seymour, IN · 47274-3342
Is this the product you have?
- Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle
- Distributed byLannett Company, Inc., Philadelphia, PA 19136
- NDC 100 Count bottle
0527-1632-01NDC 1000
- bottle0527-1632-10
- Lot codes and dates
- Lots
21000279A (exp 01/2023)20256320A (12/2022)
- Lots
- Amount recalled
- 20,040 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
Failed Impurity/Degradation Specifications
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
Want the full recall guide?
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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