United States · FDA National Drug Code directory
Naproxen and 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
- 68788-8906_470496f5-a71d-40b2-bf11-3a8d3d790962
- Product NDC
- 68788-8906
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Naproxen and esomeprazole magnesium
- Labeler
- Preferred Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250731
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN — 375 mg/1
- ESOMEPRAZOLE MAGNESIUM TRIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8906-3) · 68788-8906-3
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8906-6) · 68788-8906-6
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 →