# Lansoprazole

NDC: 0363-1419
Generic name: Lansoprazole
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20170525

FDA application: NDA208025

## Active ingredients

- LANSOPRAZOLE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-1419"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-1419
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a72f92cc-db49-40ef-a249-6b7c50dc8ef2