# Omeprazole

NDC: 71335-0569
Generic name: Omeprazole
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20031111
Marketing ended: 20270131
FDA application: ANDA076048

## 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:"71335-0569"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0569
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44349466-73ea-4053-8ff6-5b4b7372c9cd