# LANSOPRAZOLE

NDC: 72288-672
Generic name: Lansoprazole
Labeler / Manufacturer: Amazon.com Services LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260812

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:"72288-672"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72288-672
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0a7e6e0-9a76-4a5a-aed7-aa976a174c0e