NDC 70518-2941
Terbinafine 250 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-079.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078297
- On the market since
- Nov 13, 2020
- Package NDCs
70518-2941-0- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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