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
- 68462-390_5eef4592-c7ef-454c-88a9-62671fff9088
- Product NDC
- 68462-390
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211101
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68462-390-10) · 68462-390-10
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68462-390-30) · 68462-390-30
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68462-390-90) · 68462-390-90
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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