# Omeprazole

NDC: 83324-011
Generic name: Omeprazole
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20240510

FDA application: ANDA211732

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83324-011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83324-011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da09aac6-8fce-448b-98ba-1fc9bce42075