United States · FDA National Drug Code directory
Esomeprazole Magnesium
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
- 59651-562_23ef720d-d1c4-498e-b54a-ecaf96e19fcb
- Product NDC
- 59651-562
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231120
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM TRIHYDRATE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-562-01) · 59651-562-01
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-562-30) · 59651-562-30
- 10 BLISTER PACK in 1 CARTON (59651-562-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 59651-562-78
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-562-90) · 59651-562-90
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-562-99) · 59651-562-99
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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