# Azelastine Hydrochloride

NDC: 68083-287
Generic name: Azelastine Hydrochloride
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: INTRAOCULAR
Marketing started: 20200225

FDA application: ANDA210092

## 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:"68083-287"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-287
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f358cecd-284f-4d0b-806c-039465220bd2