NDC 51672-1376
Naftifine Hydrochloride 20 mg per 1 g gel
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Product details
- Generic drug
- Naftifine: every company that makes it
- Form
- gel, topical
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA208201
- On the market since
- Apr 1, 2023
- Package NDCs
51672-1376-351672-1376-6- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2026
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