# Olopatadine Hydrochloride

NDC: 73581-712
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: 20260831

FDA application: ANDA204812

## 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:"73581-712"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73581-712
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=598156e4-f183-86f5-e063-6294a90a64df