# OLOPATADINE HYDROCHLORIDE

NDC: 46122-672
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: 20210120

FDA application: ANDA204812

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46122-672"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-672
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3b054d2-4abd-4a1f-910d-0c61e2a24fbf