NDC 67046-1612
Levothyroxine Sodium 125 ug tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Lannett Company, Inc.'s NDC 0527-3286.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Neolpharma, Inc. | Caguas, PR, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 10, 2026 · 6 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet, oral
- Strength
- 125 ug
- Approval
- NDA authorized generic NDA021342
- On the market since
- Nov 7, 2025
- Package NDCs
67046-1612-3- Official label
- DailyMed (National Library of Medicine), updated Nov 7, 2025
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