United States · FDA National Drug Code directory
Medique Mediproxen
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
- 47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63
- Product NDC
- 47682-237
- Form
- TABLET, FILM COATED
- Composition / generic term
- NAPROXEN SODIUM
- Labeler
- Unifirst First Aid Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081230
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46) · 47682-237-33
- 1 TABLET, FILM COATED in 1 PACKET (47682-237-46) · 47682-237-46
- 50 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET · 47682-237-50
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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