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
70771-1392_983313a8-2120-4c76-8412-0c0c6a159465
Product NDC
70771-1392
Form
GRANULE, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
Zydus Lifesciences Limited
Marketing category
ANDA
Marketing start / end (source format)
20230630
Source listing expiry
20261231

Source-listed ingredients

  • ESOMEPRAZOLE MAGNESIUM DIHYDRATE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 GRANULE, DELAYED RELEASE in 1 CARTON (70771-1392-3) · 70771-1392-3

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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