# OLOPATADINE HYDROCHLORIDE

NDC: 73581-709
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: YYBA Corp
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20260301

FDA application: ANDA219557

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73581-709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73581-709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47f8ae9b-d92b-4bcb-e063-6294a90af45a