# LANSOPRAZOLE

NDC: 72288-827
Generic name: Lansoprazole
Labeler / Manufacturer: Amazon.com Services LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260709

FDA application: ANDA202319

## 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:"72288-827"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72288-827
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8d09f97-4c39-4aa7-a9a0-4fd2a59836bb