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
43598-509_bc23d230-ec98-ff25-5296-39e31fe9b775
Product NDC
43598-509
Form
CAPSULE, DELAYED RELEASE
Composition / generic term
Esomeprazole Magnesium
Labeler
Dr. Reddy's Laboratories Inc
Marketing category
ANDA
Marketing start / end (source format)
20151210
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 (43598-509-10) · 43598-509-10
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43598-509-30) · 43598-509-30
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43598-509-90) · 43598-509-90

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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