# OLOPATADINE HYDROCHLORIDE

NDC: 68001-674
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20251205

FDA application: ANDA219557

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-674"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-674
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e86783f-0001-625f-e063-6294a90acd20