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
51316-088_c7b8460b-d1da-41d9-b644-157718295382
Product NDC
51316-088
Form
TABLET, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
CVS Pharmacy, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240704
Source listing expiry
20261231

Source-listed ingredients

  • ESOMEPRAZOLE MAGNESIUM DIHYDRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (51316-088-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 51316-088-01
  • 3 BOTTLE in 1 CARTON (51316-088-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 51316-088-05

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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