NDC 70518-3907
terbinafine hydrochloride 250 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078163
- On the market since
- Nov 3, 2023
- Package NDCs
70518-3907-070518-3907-170518-3907-270518-3907-3- Official label
- DailyMed (National Library of Medicine), updated Jul 9, 2026
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