United States · FDA National Drug Code directory
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
- 11534-212_502c7695-7f9d-4893-b151-65111de2e2a7
- Product NDC
- 11534-212
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Naproxen
- Labeler
- Sunrise Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251209
- Source listing expiry
- 20261231
Source-listed ingredients
- NAPROXEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11534-212-01) · 11534-212-01
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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