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
- 71335-0058_b565e019-9796-48dc-ab9e-6c939bd7c08c
- Product NDC
- 71335-0058
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- lansoprazole
- Labeler
- Bryant Ranch Prepack
- 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
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-1) · 71335-0058-1
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-2) · 71335-0058-2
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-3) · 71335-0058-3
- 58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-4) · 71335-0058-4
- 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-5) · 71335-0058-5
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-6) · 71335-0058-6
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-7) · 71335-0058-7
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-8) · 71335-0058-8
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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