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
- 49483-608_0538c5c7-c559-4ea9-e063-6294a90aec21
- Product NDC
- 49483-608
- Form
- TABLET, FILM COATED
- Composition / generic term
- NAPROXEN SODIUM
- Labeler
- TIME CAP LABORATORIES, INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160328
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN SODIUM — 220 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6500 TABLET, FILM COATED in 1 BAG (49483-608-00) · 49483-608-00
- 100 TABLET, FILM COATED in 1 BOTTLE (49483-608-01) · 49483-608-01
- 50 TABLET, FILM COATED in 1 BOTTLE (49483-608-05) · 49483-608-05
- 300 TABLET, FILM COATED in 1 BOTTLE (49483-608-31) · 49483-608-31
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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