# Azelastine HCl

NDC: 69238-2147
Generic name: Azelastine
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20240607

FDA application: ANDA216576

## 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:"69238-2147"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-2147
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82610437-25f4-4ae0-9d6a-381e9932f87d