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
- 67877-478_c6b5c112-5f5b-453a-836f-54bac8c7dca9
- Product NDC
- 67877-478
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Esomeprazole magnesium
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171020
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-478-05) · 67877-478-05
- 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-478-10) · 67877-478-10
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-478-30) · 67877-478-30
- 10 BLISTER PACK in 1 CARTON (67877-478-38) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK · 67877-478-38
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-478-90) · 67877-478-90
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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