United States · FDA National Drug Code directory
All Day Pain Relief
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
- 79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83
- Product NDC
- 79903-005
- Form
- TABLET, FILM COATED
- Composition / generic term
- Naproxen Sodium
- Labeler
- WALMART INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201022
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20) · 79903-005-20
- 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25) · 79903-005-25
- 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27) · 79903-005-27
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90) · 79903-005-90
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 →