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: 58602-738_3d89b39b-8273-4715-91b1-7a8bccb458d8
Product NDC: 58602-738
Form: TABLET, FILM COATED
Composition / generic term: Naproxen Sodium
Labeler: Aurohealth LLC
Marketing category: ANDA
Marketing start / end (source format): 20160318
Source listing expiry: 20261231

Source-listed ingredients

NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (58602-738-07) / 24 TABLET, FILM COATED in 1 BOTTLE · 58602-738-07
1 BOTTLE in 1 CARTON (58602-738-12) / 40 TABLET, FILM COATED in 1 BOTTLE · 58602-738-12
1 BOTTLE in 1 CARTON (58602-738-14) / 50 TABLET, FILM COATED in 1 BOTTLE · 58602-738-14
1 BOTTLE in 1 CARTON (58602-738-19) / 90 TABLET, FILM COATED in 1 BOTTLE · 58602-738-19
1 BOTTLE in 1 CARTON (58602-738-21) / 100 TABLET, FILM COATED in 1 BOTTLE · 58602-738-21
1 BOTTLE in 1 CARTON (58602-738-25) / 130 TABLET, FILM COATED in 1 BOTTLE · 58602-738-25
1 BOTTLE in 1 CARTON (58602-738-29) / 150 TABLET, FILM COATED in 1 BOTTLE · 58602-738-29
1 BOTTLE in 1 CARTON (58602-738-34) / 200 TABLET, FILM COATED in 1 BOTTLE · 58602-738-34
300 TABLET, FILM COATED in 1 BOTTLE (58602-738-38) · 58602-738-38
500 TABLET, FILM COATED in 1 BOTTLE (58602-738-40) · 58602-738-40
400 TABLET, FILM COATED in 1 BOTTLE (58602-738-44) · 58602-738-44

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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