Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-040-20
Reported: December 18, 2024 Initiated: November 19, 2024 #D-0136-2025
Product Description
Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-040-20
Reason for Recall
Subpotent and Superpotent Drug
Details
- Recalling Firm
- Mylan Institutional, Inc.
- Units Affected
- 205 cartons
- Distribution
- Nationwide in the USA.
- Location
- Rockford, IL
Frequently Asked Questions
What product was recalled? ▼
Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-040-20. Recalled by Mylan Institutional, Inc.. Units affected: 205 cartons.
Why was this product recalled? ▼
Subpotent and Superpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 18, 2024. Severity: Moderate. Recall number: D-0136-2025.
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