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
- 69230-329_ee21e0f7-9f32-6c63-e053-2a95a90ac996
- Product NDC
- 69230-329
- Form
- TABLET, FILM COATED
- Composition / generic term
- Naproxen sodium
- Labeler
- Camber Consumer Care Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221028
- 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 (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLE · 69230-329-01
- 1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLE · 69230-329-02
- 500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05) · 69230-329-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10) · 69230-329-10
- 1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLE · 69230-329-24
- 1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE · 69230-329-50
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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