NDC 50090-7300
terbinafine hydrochloride 250 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Bionpharma Inc.'s NDC 69452-351.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| OrBion Pharmaceuticals Private Limited | Kancheepuram, India | Makes it, tests it, packages it and labels it | No problems foundOct 27, 2025 · 6 inspections |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078163
- On the market since
- Jan 28, 2022
- Package NDCs
50090-7300-050090-7300-1- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2024
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