NDC 51655-364
Terbinafine Hydrochloride 250 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-526.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Laboratorios Liconsa SAU | Azuqueca De Henares, Spain | Makes it | Problems found, fixed voluntarilyJan 17, 2025 · 6 inspections |
| Apace Packaging LLC | Fountain Run, KY, United States | Packages it | No problems foundJan 13, 2022 · 6 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA077714
- On the market since
- May 28, 2020
- Package NDCs
51655-364-26- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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