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
- 71335-3075_405bbf1d-085e-461b-9b57-102cafa88a4f
- Product NDC
- 71335-3075
- Form
- TABLET
- Composition / generic term
- Naproxen Sodium
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070801
- 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 (71335-3075-0) · 71335-3075-0
- 20 TABLET in 1 BOTTLE (71335-3075-1) · 71335-3075-1
- 100 TABLET in 1 BOTTLE (71335-3075-2) · 71335-3075-2
- 30 TABLET in 1 BOTTLE (71335-3075-3) · 71335-3075-3
- 120 TABLET in 1 BOTTLE (71335-3075-4) · 71335-3075-4
- 60 TABLET in 1 BOTTLE (71335-3075-5) · 71335-3075-5
- 90 TABLET in 1 BOTTLE (71335-3075-6) · 71335-3075-6
- 42 TABLET in 1 BOTTLE (71335-3075-7) · 71335-3075-7
- 14 TABLET in 1 BOTTLE (71335-3075-8) · 71335-3075-8
- 56 TABLET in 1 BOTTLE (71335-3075-9) · 71335-3075-9
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 →