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
71335-1425_40271c8f-06d7-42c1-a983-8d49f0205268
Product NDC
71335-1425
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Lansoprazole
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180604
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 (71335-1425-1) · 71335-1425-1
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-2) · 71335-1425-2
  • 18 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-3) · 71335-1425-3
  • 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-4) · 71335-1425-4
  • 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-5) · 71335-1425-5
  • 58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-6) · 71335-1425-6
  • 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-7) · 71335-1425-7
  • 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-8) · 71335-1425-8
  • 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1425-9) · 71335-1425-9

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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