United States · FDA National Drug Code directory
Dexlansoprazole
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
- 0378-2086_bd08545b-3f1d-44c5-bdd9-05acd7f69a0a
- Product NDC
- 0378-2086
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- dexlansoprazole
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240122
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXLANSOPRAZOLE SESQUIHYDRATE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-77) · 0378-2086-77
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-93) · 0378-2086-93
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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