# up and up omeprazole

NDC: 11673-346
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: 20220203

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:"11673-346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7dc339da-e90b-452b-b25e-8d7f3aa8bc18