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
- 55111-739_06355b28-9bb0-baea-0f4b-f1e4f7e670b6
- Product NDC
- 55111-739
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Lansoprazole
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190819
- Source listing expiry
- 20271231
Source-listed ingredients
- LANSOPRAZOLE — 15 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (55111-739-27) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-739-27
- 3 BOTTLE in 1 CARTON (55111-739-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-739-33
- 1 BOTTLE in 1 CARTON (55111-739-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 55111-739-52
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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