# OLOPATADINE HYDROCHLORIDE

NDC: 72657-194
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: GLENMARK THERAPEUTICS INC., USA
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20250228

FDA application: ANDA219557

## 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:"72657-194"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72657-194
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07e8b359-d4ae-4b5b-81dc-c7e57e172c58