FDA NDC Directory · JSON-LD · Markdown

Oxymetazoline Hydrochloride

NDC 51672-1405 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213584
Dosage form / routeCREAM · TOPICAL
Active ingredientsOXYMETAZOLINE HYDROCHLORIDE (10 mg/g)
Marketing started20260715
Package count2

External sources

Source: openFDA. Public-domain (CC0).