FDAFDA · Food and drugs·Recall number D-0167-2025
Levothyroxine Sodium Tablets, Lupin, 75 mcg (0.075mg), 1000 Tablets, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited, Pithampur (M.P)- 454 775 INDIA, NDC# 68180-967-03
Published January 8, 2025 · Recall initiated: December 20, 2024
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- LEVOTHYROXINE SODIUM
- Manufacturer
- Lupin Pharmaceuticals Inc.
- Distributor
- One US distributor in Ohio.
- UPC
- 0368180973010
- Lot
- Lot# LA01276, Exp Date: 07/2026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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