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
- 71205-479_397db794-027c-4a89-993e-07c208b457a3
- Product NDC
- 71205-479
- Form
- TABLET, FILM COATED
- Composition / generic term
- Naproxen Sodium
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111031
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 550 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (71205-479-15) · 71205-479-15
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-479-30) · 71205-479-30
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-479-60) · 71205-479-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-479-90) · 71205-479-90
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 →