NDC 67046-1679
Levothyroxine Sodium 100 ug tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-397.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | Valsad, India | Makes it, makes the active ingredient, tests it, packages it, labels it and mills it | Problems found, fixed voluntarilyAug 4, 2026 · 5 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Recalls
- Feb 26, 2026 · Class II · Macleods Pharma Usa, Inc
Subpotent Drug
Lots: Lot 16240062A, exp date 3/2026 - May 29, 2025 · Class III · Macleods Pharmaceuticals Ltd
Presence of a foreign substance: black hair found embedded in tablet.
Lots: Lot #: MLF2401A, Exp 01/31/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet, oral
- Strength
- 100 ug
- Approval
- ANDA ANDA211417
- On the market since
- Jun 5, 2026
- Package NDCs
67046-1679-3- Official label
- DailyMed (National Library of Medicine), updated Jun 5, 2026
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