# Omeprazole

NDC: 59726-744
Generic name: Omeprazole
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250829

FDA application: ANDA206582

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59726-744"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-744
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=883e428a-e157-4bbf-8657-e7a93dc99e8c