NDC 51672-1362
Naftifine Hydrochloride 10 mg per 1 g cream
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
- cream, topical
- Strength
- 10 mg per 1 g
- Approval
- ANDA ANDA205975
- On the market since
- Sep 8, 2016
- Package NDCs
51672-1362-151672-1362-251672-1362-351672-1362-8- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2025
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