United States · FDA National Drug Code directory
Flanax Pain Reliever/Fever Reducer
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
- 27854-700_4215c852-11ed-4b06-b132-3674265078e3
- Product NDC
- 27854-700
- Form
- TABLET, FILM COATED
- Composition / generic term
- Naproxen sodium
- Labeler
- Belmora LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200515
- 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 (27854-700-01) / 24 TABLET, FILM COATED in 1 BOTTLE · 27854-700-01
- 1 BOTTLE in 1 CARTON (27854-700-10) / 10 TABLET, FILM COATED in 1 BOTTLE · 27854-700-10
- 1 BOTTLE in 1 CARTON (27854-700-99) / 100 TABLET, FILM COATED in 1 BOTTLE · 27854-700-99
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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