# Azelastine Hydrochloride

NDC: 47335-938
Generic name: Azelastine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: INTRAOCULAR
Marketing started: 20100531

FDA application: ANDA078738

## Active ingredients

- AZELASTINE HYDROCHLORIDE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-938"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-938
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04e5eede-17ff-4765-af77-d46c139da703