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
0363-0361_c6e874bf-fe37-4820-ab9c-224e8daa1194
Product NDC
0363-0361
Form
TABLET, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
WALGREEN CO.
Marketing category
ANDA
Marketing start / end (source format)
20240708
Source listing expiry
20261231

Source-listed ingredients

  • ESOMEPRAZOLE MAGNESIUM DIHYDRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BOTTLE in 1 CARTON (0363-0361-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 0363-0361-42

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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