United States · FDA National Drug Code directory
Naproxen
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
- 71335-2777_7218d46c-3db2-4c6e-8b5b-58b8d576d4d0
- Product NDC
- 71335-2777
- Form
- TABLET
- Composition / generic term
- Naproxen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111108
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET in 1 BOTTLE (71335-2777-0) · 71335-2777-0
- 30 TABLET in 1 BOTTLE (71335-2777-1) · 71335-2777-1
- 60 TABLET in 1 BOTTLE (71335-2777-2) · 71335-2777-2
- 10 TABLET in 1 BOTTLE (71335-2777-3) · 71335-2777-3
- 90 TABLET in 1 BOTTLE (71335-2777-4) · 71335-2777-4
- 20 TABLET in 1 BOTTLE (71335-2777-5) · 71335-2777-5
- 120 TABLET in 1 BOTTLE (71335-2777-6) · 71335-2777-6
- 14 TABLET in 1 BOTTLE (71335-2777-7) · 71335-2777-7
- 42 TABLET in 1 BOTTLE (71335-2777-8) · 71335-2777-8
- 40 TABLET in 1 BOTTLE (71335-2777-9) · 71335-2777-9
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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