# MOMETASONE FUROATE

NDC: 58602-522
Generic name: MOMETASONE FUROATE
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20241122

FDA application: ANDA217498

## Active ingredients

- MOMETASONE FUROATE MONOHYDRATE: 50 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-522"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-522
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48ba8c52-73b6-4ee9-ba13-756a645a9183