# Azelastine Hydrochloride

NDC: 65162-676
Generic name: Azelastine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20170905

FDA application: ANDA204660

## Active ingredients

- AZELASTINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-676"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-676
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7902605c-944a-4d7e-a7d4-eb4a71bcacdb