NDC 51991-526
Terbinafine Hydrochloride 250 mg tablet
On the label: Breckenridge Pharmaceutical, Inc..
Where it's 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 |
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA077714
- On the market since
- Dec 27, 2010
- Package NDCs
51991-526-0151991-526-33- Official label
- DailyMed (National Library of Medicine), updated Dec 22, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?