NDC 51672-1368 – Naftifine Hydrochloride
Naftifine Hydrochloride 20 mg/g · Cream · Topical
Product NDC51672-1368
Product details
- Brand name
- Naftifine Hydrochloride
- Generic name
- Naftifine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- ANDA · ANDA206901
- Marketed since
- January 6, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Allylamine Antifungal
Active ingredients
- Naftifine Hydrochloride 20 mg/g
Uses, dosage, side effects and warnings for Naftifine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1368-2 | 1 TUBE in 1 CARTON (51672-1368-2) / 30 g in 1 TUBE | Jan 6, 2016 |
| 51672-1368-3 | 1 TUBE in 1 CARTON (51672-1368-3) / 60 g in 1 TUBE | Jan 6, 2016 |
| 51672-1368-6 | 1 TUBE in 1 CARTON (51672-1368-6) / 45 g in 1 TUBE | Jan 6, 2016 |
Other Naftifine Hydrochloride products
- 51672-1362 Naftifine Hydrochloride 10 mg/g · Cream · Sun Pharmaceutical Industries, Inc.
- 51672-1376 Naftifine Hydrochloride 20 mg/g · Gel · Sun Pharmaceutical Industries, Inc.