United States · FDA National Drug Code directory
Naproxen Sodium
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
- 71335-9663_991ca4e2-175c-457d-b2e6-62b1cb17e7f3
- Product NDC
- 71335-9663
- Form
- TABLET
- Composition / generic term
- Naproxen Sodium
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191030
- Source listing expiry
- 20271231
Source-listed ingredients
- NAPROXEN SODIUM — 550 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (71335-9663-0) · 71335-9663-0
- 20 TABLET in 1 BOTTLE (71335-9663-1) · 71335-9663-1
- 100 TABLET in 1 BOTTLE (71335-9663-2) · 71335-9663-2
- 30 TABLET in 1 BOTTLE (71335-9663-3) · 71335-9663-3
- 120 TABLET in 1 BOTTLE (71335-9663-4) · 71335-9663-4
- 60 TABLET in 1 BOTTLE (71335-9663-5) · 71335-9663-5
- 90 TABLET in 1 BOTTLE (71335-9663-6) · 71335-9663-6
- 42 TABLET in 1 BOTTLE (71335-9663-7) · 71335-9663-7
- 14 TABLET in 1 BOTTLE (71335-9663-8) · 71335-9663-8
- 56 TABLET in 1 BOTTLE (71335-9663-9) · 71335-9663-9
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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