# MOMETASONE FUROATE MONOHYDRATE

NDC: 59651-402
Generic name: MOMETASONE FUROATE MONOHYDRATE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20240318

FDA application: ANDA215878

## 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:"59651-402"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-402
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b24f80c5-afe2-4821-9185-2dad3cfe277a