# up and up omeprazole

NDC: 11673-212
Generic name: omeprazole
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180509

FDA application: NDA209400

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11673-212"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-212
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f2eb5e8-80f2-4c40-a8ad-e1d9c10d0c56