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
- 21130-100_a687eeae-996e-4641-80a3-930db64689d7
- Product NDC
- 21130-100
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- Better Living Brands LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190724
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM DIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (21130-100-05) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 21130-100-05
- 2 BOTTLE in 1 CARTON (21130-100-08) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 21130-100-08
- 3 BOTTLE in 1 CARTON (21130-100-10) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 21130-100-10
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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