# omeprazole

NDC: 37808-354
Generic name: omeprazole
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20180305

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:"37808-354"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-354
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=344b5548-e5c0-45bf-bc3f-73af50bd5913