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
- 75907-119_a40c48e8-93c4-8b65-6b4d-a6d236e39c38
- Product NDC
- 75907-119
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Esomeprazole Magnesium
- Labeler
- Dr. Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231230
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (75907-119-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 75907-119-27
- 3 BOTTLE in 1 CARTON (75907-119-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 75907-119-33
- 1 BOTTLE in 1 CARTON (75907-119-52) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE · 75907-119-52
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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