NDC 68071-2579
Terbinafine 250 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-795.
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 |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA078297
- On the market since
- Jul 2, 2007
- Package NDCs
68071-2579-3- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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