# OLOPATADINE HYDROCHLORIDE

NDC: 76162-020
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: TOPCO ASSOCIATES LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20200715

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:"76162-020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76162-020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f5bddc73-1899-b5f0-e053-2995a90ab98f