# Azelastine Hydrochloride

NDC: 50090-2330
Generic name: azelastine hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20100301

FDA application: ANDA077954

## 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:"50090-2330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-2330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02257284-4bb1-4fe6-8134-e5a67a645114