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
50090-6154_32579728-eb82-4ea8-bf4c-8bc5bdc4483f
Product NDC
50090-6154
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Lansoprazole
Labeler
A-S Medication Solutions
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 (50090-6154-0) · 50090-6154-0
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6154-1) · 50090-6154-1

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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