# OLOPATADINE HYDROCHLORIDE

NDC: 70069-491
Generic name: Olopatadine Hydrochloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20241220

FDA application: ANDA215006

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-491"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-491
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6ee9f8f5-973c-4c71-8069-e76cd87b07dc