# omeprazole

NDC: 37808-915
Generic name: Omeprazole
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20080229

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:"37808-915"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-915
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5ceaec04-3ca3-4c7c-9184-51a42686a595