# OLOPATADINE HYDROCHLORIDE

NDC: 72476-851
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: Retail Business Services, LLC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20210402

FDA application: ANDA209995

## 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:"72476-851"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72476-851
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bca27f6a-d1b1-1d6a-e053-2995a90a37b5