D-0135-2025 Class II Ongoing

Recalled by Mylan Institutional, Inc. — Rockford, IL

FDA drug recall D-0135-2025 was initiated by Mylan Institutional, Inc. on Nov 19, 2024 and is designated Class II. Reason for recall: Subpotent and Superpotent Drug The recall status is ongoing. Affected quantity: 690 cartons.

Recall Details

Product Type
Drugs
Report Date
Dec 18, 2024
Initiation Date
Nov 19, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
690 cartons

Product Description

Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 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: 51079-445-20

Reason for Recall

Subpotent and Superpotent Drug

Distribution Pattern

Nationwide in the USA.

Code Information

Lot #: 3115924, Exp. Date 06/2025

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0135-2025
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for D-0135-2025. Report a data issue: hello@regdatalab.com.