# Azelastine Hydrochloride

NDC: 47335-779
Generic name: Azelastine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20120524

FDA application: ANDA090423

## Active ingredients

- AZELASTINE HYDROCHLORIDE: 137 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-779"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-779
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=305c6dc8-8247-473d-9975-b02903af6d53