# Azelastine Hydrochloride

NDC: 71205-449
Generic name: azelastine hydrochloride
Labeler / Manufacturer: Proficient Rx LP
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-449"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-449
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11a74cae-a15b-4a6b-a8c0-1e6a234ee258