# Omeprazole Delayed-Release

NDC: 37808-569
Generic name: Omeprazole
Labeler / Manufacturer: H-E-B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260701

FDA application: ANDA218829

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-569"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-569
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=448ba584-6a6e-3d85-e063-6294a90a5579