# up and up omeprazole

NDC: 11673-915
Generic name: Omeprazole
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20090714

FDA application: NDA022032

## 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:"11673-915"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-915
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f2b26fe-dbc2-4185-8a27-6b166dd49ba2