# Omeprazole DR

NDC: 80425-0169
Generic name: Omeprazole
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20141031

FDA application: ANDA091672

## Active ingredients

- OMEPRAZOLE: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8bf92c9-1bab-7985-e053-2995a90a0225