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
- 71335-1820_e66cf5f3-d909-40ad-a03d-c0423f41aa23
- Product NDC
- 71335-1820
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Lansoprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180824
- Source listing expiry
- 20261231
Source-listed ingredients
- LANSOPRAZOLE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-1) · 71335-1820-1
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-2) · 71335-1820-2
- 18 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-3) · 71335-1820-3
- 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-4) · 71335-1820-4
- 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-5) · 71335-1820-5
- 58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-6) · 71335-1820-6
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-7) · 71335-1820-7
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-8) · 71335-1820-8
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-9) · 71335-1820-9
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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