# Olopatadine Hydrochloride

NDC: 62332-709
Generic name: olopatadine hydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20210218

FDA application: ANDA209919

## 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:"62332-709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd1f9779-d048-46ff-a570-ce3ad92715e7