# Olopatadine hydrochloride

NDC: 60505-6221
Generic name: Olopatadine hydrochloride
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20221006

FDA application: ANDA078350

## 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:"60505-6221"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6221
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc178825-1a4e-6bca-a00d-aa28d5abe589