# Olopatadine Hydrochloride

NDC: 0536-1307
Generic name: Olopatadine Hydrochloride
Labeler / Manufacturer: Rugby Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20210115

FDA application: ANDA209752

## 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:"0536-1307"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0536-1307
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95424539-7883-2da3-8a46-3d1a19259e15