# Olopatadine

NDC: 70069-017
Generic name: Olopatadine
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20240415

FDA application: ANDA206306

## 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:"70069-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55142e80-c5db-46a5-85a5-e8a040bcc8cf