# Olopatadine Hydrochloride

NDC: 46708-709
Generic name: olopatadine hydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
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:"46708-709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac82e6ea-5694-4f48-819b-91fc567ceaf1