# omeprazole

NDC: 42507-164
Generic name: omeprazole
Labeler / Manufacturer: HyVee Inc
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260128

FDA application: NDA209400

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42507-164"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42507-164
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd22d4df-9679-4c2d-9bc4-3619288fb4cc