# omeprazole

NDC: 72559-014
Generic name: omeprazole
Labeler / Manufacturer: Little Pharma, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200715

FDA application: ANDA207891

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72559-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72559-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4f86bbe-fe4d-41e2-96cc-4b4bbe2f1f7f