# Azelastine Hydrochloride and Fluticasone Propionate

NDC: 0480-2157
Generic name: Azelastine Hydrochloride and Fluticasone Propionate
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20250908

FDA application: ANDA208436

## Active ingredients

- AZELASTINE HYDROCHLORIDE: 137 ug/1
- FLUTICASONE PROPIONATE: 50 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-2157"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-2157
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0d45e7a4-900f-44ef-bb18-a1fbff75a3c6