NDC 51655-537
Levothyroxine Sodium 175 ug tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Lannett Company, Inc.'s NDC 0527-3289.
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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Levothyroxine: every company that makes it
- Form
- tablet, oral
- Strength
- 175 ug
- Approval
- NDA authorized generic NDA021342
- On the market since
- Dec 28, 2022
- Package NDCs
51655-537-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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