# olopatadine hydrochloride

NDC: 16571-861
Generic name: olopatadine hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20250501

FDA application: ANDA204620

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-861"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-861
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0988e6e2-59a9-47dc-9386-9e9ea877e6c1