Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10
Reported: January 25, 2023 Initiated: November 9, 2022 #D-0161-2023
Product Description
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10
Reason for Recall
Failed Impurity/Degradation Specifications
Details
- Recalling Firm
- Lannett Company Inc.
- Units Affected
- 20,040 bottles
- Distribution
- Nationwide USA
- Location
- Seymour, IN
Frequently Asked Questions
What product was recalled? ▼
Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10. Recalled by Lannett Company Inc.. Units affected: 20,040 bottles.
Why was this product recalled? ▼
Failed Impurity/Degradation Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 25, 2023. Severity: Low. Recall number: D-0161-2023.
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