# OLOPATADINE HYDROCHLORIDE

NDC: 46122-671
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: Amerisource Bergen
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20210119

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:"46122-671"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-671
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=067baa0b-5c01-4908-92de-ad79c73d2c37
