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
70000-0695_90df7bbb-c55e-4a01-90b7-c118b65617a9
Product NDC
70000-0695
Form
TABLET, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
Cardinal Health
Marketing category
ANDA
Marketing start / end (source format)
20240627
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 (70000-0695-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 70000-0695-1
  • 3 BOTTLE in 1 CARTON (70000-0695-2) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 70000-0695-2

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →