United States · FDA National Drug Code directory
LANSOPRAZOLE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72288-672_118fc2cf-cc34-49cf-944a-da4f41b69601
- Product NDC
- 72288-672
- Form
- TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
- Composition / generic term
- Lansoprazole
- Labeler
- Amazon.com Services LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20260812
- Source listing expiry
- 20271231
Source-listed ingredients
- LANSOPRAZOLE — 15 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 CARTON in 1 CARTON (72288-672-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK · 72288-672-55
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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