# omeprazole

NDC: 0363-6101
Generic name: omeprazole
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230309

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:"0363-6101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-6101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87cee50d-4c1e-473d-9d70-b1622f84aee1