United States · FDA National Drug Code directory
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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
- 0363-9608_13aeca7d-1120-844d-e063-6294a90ac3d9
- Product NDC
- 0363-9608
- Form
- TABLET, COATED
- Composition / generic term
- NAPROXEN SODIUM
- Labeler
- WALGREENS
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190626
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET, COATED in 1 BOTTLE (0363-9608-05) · 0363-9608-05
- 1 BOTTLE in 1 CARTON (0363-9608-09) / 90 TABLET, COATED in 1 BOTTLE · 0363-9608-09
- 200 TABLET, COATED in 1 BOTTLE (0363-9608-20) · 0363-9608-20
- 270 TABLET, COATED in 1 BOTTLE (0363-9608-27) · 0363-9608-27
- 1 BOTTLE in 1 CARTON (0363-9608-42) / 24 TABLET, COATED in 1 BOTTLE · 0363-9608-42
- 600 TABLET, COATED in 1 BOTTLE (0363-9608-61) · 0363-9608-61
- 90 TABLET, COATED in 1 BOTTLE (0363-9608-90) · 0363-9608-90
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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