# Omeprazole

NDC: 68788-8864
Generic name: Omeprazole
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250423

FDA application: ANDA075757

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8864"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8864
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0fb314cb-6291-422c-98ff-24d8449992f6