# Once Daily Relief

NDC: 37808-045
Generic name: Olopatadine Hydrochloride Ophthalmic Solution
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20220307

FDA application: ANDA209752

## 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:"37808-045"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-045
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0cb0bb66-def2-35d4-7fe0-987757095d08