United States · FDA National Drug Code directory

Care One 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
41520-533_38ff98c9-997e-4382-a7a7-ce3702fe2ae4
Product NDC
41520-533
Form
TABLET, FILM COATED
Composition / generic term
Naproxen Sodium
Labeler
American Sales Company
Marketing category
ANDA
Marketing start / end (source format)
20160708
Source listing expiry
20271231

Source-listed ingredients

  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (41520-533-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 41520-533-71

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 →