# OMEPRAZOLE

NDC: 59640-699
Generic name: Omeprazole
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260807

FDA application: ANDA216096

## 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:"59640-699"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59640-699
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4eb05eb3-be59-4132-95a8-5a8f5065d758