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
- 55111-398_c8eb1d41-1fd2-7c06-486c-e6abf08faa6d
- Product NDC
- 55111-398
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- lansoprazole
- Labeler
- Dr.Reddy's Laboratories Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101015
- Source listing expiry
- 20261231
Source-listed ingredients
- LANSOPRAZOLE — 15 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-01) · 55111-398-01
- 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-05) · 55111-398-05
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-30) · 55111-398-30
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-60) · 55111-398-60
- 1 BLISTER PACK in 1 CARTON (55111-398-79) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 55111-398-79
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-398-90) · 55111-398-90
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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