United States · FDA National Drug Code directory
Naproxen Sodium BACK AND MUSCLE PAIN
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
- 58602-736_c640a53f-e070-4393-ba97-21c4c7c526e5
- Product NDC
- 58602-736
- Form
- TABLET, FILM COATED
- Composition / generic term
- Naproxen Sodium
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210714
- 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 (58602-736-07) / 24 TABLET, FILM COATED in 1 BOTTLE · 58602-736-07
- 1 BOTTLE in 1 CARTON (58602-736-19) / 90 TABLET, FILM COATED in 1 BOTTLE · 58602-736-19
- 1 BOTTLE in 1 CARTON (58602-736-21) / 100 TABLET, FILM COATED in 1 BOTTLE · 58602-736-21
- 1 BOTTLE in 1 CARTON (58602-736-29) / 150 TABLET, FILM COATED in 1 BOTTLE · 58602-736-29
- 1 BOTTLE in 1 CARTON (58602-736-38) / 300 TABLET, FILM COATED in 1 BOTTLE · 58602-736-38
- 1 BOTTLE in 1 CARTON (58602-736-40) / 500 TABLET, FILM COATED in 1 BOTTLE · 58602-736-40
- 1 BOTTLE in 1 CARTON (58602-736-78) / 50 TABLET, FILM COATED in 1 BOTTLE · 58602-736-78
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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