# AZELASTINE HYDROCHLORIDE

NDC: 73581-500
Generic name: AZELASTINE HYDROCHLORIDE
Labeler / Manufacturer: YYBA Corp
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20260714

FDA application: ANDA216561

## Active ingredients

- AZELASTINE HYDROCHLORIDE: 205.5 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73581-500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73581-500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52f67910-11a7-6e7d-e063-6394a90ac9e8
