NDC 51672-1405 – Oxymetazoline Hydrochloride

Oxymetazoline Hydrochloride 10 mg/g · Cream · Topical

Human Prescription Drug

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

Uses, dosage, side effects and warnings for Oxymetazoline Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1405-21 TUBE in 1 CARTON (51672-1405-2) / 30 g in 1 TUBEJul 15, 2026
51672-1405-31 TUBE in 1 CARTON (51672-1405-3) / 60 g in 1 TUBEJul 15, 2026

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