# Azelastine Hydrochloride

NDC: 51316-840
Generic name: Azelastine Hydrochloride
Labeler / Manufacturer: CVS PHARMACY, INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20250801

FDA application: ANDA216421

## 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:"51316-840"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51316-840
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22d516d0-da22-4e3b-a4a5-135b009bc968