Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10

Class I - Dangerous
💊 Drugs Recalled: November 9, 2022 Lannett Company Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lots: 20256318A (12/2022), 20256321A (12/2022), 21000238A (01/2023)
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Lannett Company Inc.
Reason for Recall:
Failed Impurity/Degradation Specifications
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10

Product Codes/Lot Numbers:

Lots: 20256318A (12/2022), 20256321A (12/2022), 21000238A (01/2023)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0160-2023

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