United States · FDA National Drug Code directory
Dexlansoprazole delayed release
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
- 72162-2239_7be7b733-4992-4eb4-9cb3-d240a878d371
- Product NDC
- 72162-2239
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- dexlansoprazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221201
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXLANSOPRAZOLE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2239-3) · 72162-2239-3
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2239-9) · 72162-2239-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →