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
76420-904_2cbe433d-9180-e5aa-e063-6394a90a452d
Product NDC
76420-904
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
Asclemed USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200602
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 in 1 BOTTLE (76420-904-00) · 76420-904-00
  • 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-904-01) · 76420-904-01
  • 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-904-12) · 76420-904-12
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-904-30) · 76420-904-30
  • 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-904-60) · 76420-904-60
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-904-90) · 76420-904-90

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 →