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
- 71335-0095_59c90ed3-0908-4977-bb00-7f102e6d7aff
- Product NDC
- 71335-0095
- Form
- TABLET
- Composition / generic term
- Naproxen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070701
- Source listing expiry
- 20271231
Source-listed ingredients
- NAPROXEN — 375 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-0095-1) · 71335-0095-1
- 30 TABLET in 1 BOTTLE (71335-0095-2) · 71335-0095-2
- 40 TABLET in 1 BOTTLE (71335-0095-3) · 71335-0095-3
- 120 TABLET in 1 BOTTLE (71335-0095-4) · 71335-0095-4
- 60 TABLET in 1 BOTTLE (71335-0095-5) · 71335-0095-5
- 90 TABLET in 1 BOTTLE (71335-0095-6) · 71335-0095-6
- 14 TABLET in 1 BOTTLE (71335-0095-7) · 71335-0095-7
- 15 TABLET in 1 BOTTLE (71335-0095-8) · 71335-0095-8
- 21 TABLET in 1 BOTTLE (71335-0095-9) · 71335-0095-9
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 →