NDC 51672-1405 – Oxymetazoline Hydrochloride
Oxymetazoline Hydrochloride 10 mg/g · Cream · Topical
Product NDC51672-1405
Product details
- Brand name
- Oxymetazoline Hydrochloride
- Generic name
- Oxymetazoline Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- ANDA · ANDA213584
- Marketed since
- July 15, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Vasoconstrictor
Active ingredients
- Oxymetazoline Hydrochloride 10 mg/g
Uses, dosage, side effects and warnings for Oxymetazoline Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1405-2 | 1 TUBE in 1 CARTON (51672-1405-2) / 30 g in 1 TUBE | Jul 15, 2026 |
| 51672-1405-3 | 1 TUBE in 1 CARTON (51672-1405-3) / 60 g in 1 TUBE | Jul 15, 2026 |
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