# Omeprazole

NDC: 82009-022
Generic name: Omeprazole
Labeler / Manufacturer: Quallent Pharmaceuticals Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20221115
Marketing ended: 20280830
FDA application: ANDA075576

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82009-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=665e9877-85ac-fdb6-54ac-1c47941ceab8