# OLOPATADINE HYDROCHLORIDE

NDC: 58602-007
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20200715

FDA application: ANDA209995

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b022f8f9-ad3d-4a6d-96aa-24c1ccd1f422