# AZELASTINE HYDROCHLORIDE

NDC: 68788-8514
Generic name: AZELASTINE HYDROCHLORIDE
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20230901

FDA application: ANDA212289

## Active ingredients

- AZELASTINE HYDROCHLORIDE: 137 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8514"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8514
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=37c40f8d-269c-4df8-8ac7-cbe78f4ca5c4