United States · FDA National Drug Code directory
Esomeprazole
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
- 57483-900_8f25bf5e-bf0d-413e-8f91-d3537939592b
- Product NDC
- 57483-900
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- esomeprazole magnesium
- Labeler
- INNOVUS PHARMACEUTICALS, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200814
- Source listing expiry
- 20261231
Source-listed ingredients
- ESOMEPRAZOLE MAGNESIUM TRIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BOTTLE in 1 CARTON (57483-900-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 57483-900-42
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 →