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
- 37808-646_50947259-d8ed-0a77-e063-6294a90a9ac8
- Product NDC
- 37808-646
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- H-E-B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260701
- Source listing expiry
- 20271231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BOTTLE in 1 CARTON (37808-646-41) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 37808-646-41
- 1 BOTTLE in 1 CARTON (37808-646-45) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 37808-646-45
- 2 BOTTLE in 1 CARTON (37808-646-82) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 37808-646-82
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 →