# Omeprazole

NDC: 62175-114
Generic name: omeprazole
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20030903

FDA application: ANDA075410

## Active ingredients

- OMEPRAZOLE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62175-114"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62175-114
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92201fb1-4570-42db-8da3-3b8c0e291d32