# Omeprazole Delayed release

NDC: 61269-720
Generic name: Omeprazole
Labeler / Manufacturer: H2-Pharma, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260804

FDA application: ANDA206582

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61269-720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61269-720