# OLOPATADINE HYDROCHLORIDE

NDC: 72657-168
Generic name: Olopatadine Hydrochloride ophthalmic
Labeler / Manufacturer: GLENMARK THERAPEUTICS INC., USA
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20240726

FDA application: ANDA200810

## 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:"72657-168"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72657-168
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a80c3fd2-47b7-4ed0-b862-9c5099684607