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approval · primary record

NAPROXEN SODIUM

FDA · NDA · 2024-11-21

AgencyFDA
Submission typeNDA
Action date2024-11-21
BrandTREXIMET
SponsorAZURITY
RouteORAL

Provenance

  • Source: openFDA Drugs@FDA
  • Fetched at: 2026-10-28T02:35:07.460Z
  • Licence class: public-domain
  • Verdict: primary-source
  • Entity id: FDA:NAPROXEN SODIUM:2024-11-21

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NAPROXEN SODIUM — approval | AEaH