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
- 68071-3735_33dd409c-d59c-d1e3-e063-6294a90a0ffb
- Product NDC
- 68071-3735
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190917
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3735-3) · 68071-3735-3
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3735-6) · 68071-3735-6
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 →