United States · FDA National Drug Code directory
Rapidol Naproxen
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
- 55758-048_4d7ad592-5b3b-e731-e063-6394a90a11e0
- Product NDC
- 55758-048
- Form
- TABLET, COATED
- Composition / generic term
- Naproxen sodium
- Labeler
- Pharmadel LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191009
- Source listing expiry
- 20271231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, COATED in 1 PACKET (55758-048-02) · 55758-048-02
- 1 BOTTLE in 1 CARTON (55758-048-24) / 24 TABLET, COATED in 1 BOTTLE · 55758-048-24
- 25 PACKET in 1 CARTON (55758-048-50) / 2 TABLET, COATED in 1 PACKET (55758-048-02) · 55758-048-50
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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