# omeprazole

NDC: 0363-1819
Generic name: omeprazole
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180301

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:"0363-1819"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-1819
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=064f048c-eddd-4370-9ee4-706f9f00c8d2