# OLOPATADINE HYDROCHLORIDE

NDC: 68001-530
Generic name: OLOPATADINE HYDROCHLORIDE
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20220408

FDA application: ANDA209995

## 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:"68001-530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dbd28ee2-bbb5-a4b1-e053-2a95a90afff4