# Oxymetazoline Hydrochloride

NDC: 51672-1405
Generic name: Oxymetazoline Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20260715

FDA application: ANDA213584

## Active ingredients

- OXYMETAZOLINE HYDROCHLORIDE: 10 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1405"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1405
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8a7f2400-5e18-4215-8d2c-f55881706107