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approval · primary record

HEPARIN SODIUM

FDA · NDA · 2025-11-19

AgencyFDA
Submission typeNDA
Action date2025-11-19
BrandHEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
SponsorHOSPIRA
RouteINJECTION

Provenance

  • Source: openFDA Drugs@FDA
  • Fetched at: 2026-10-28T02:35:20.475Z
  • Licence class: public-domain
  • Verdict: primary-source
  • Entity id: FDA:HEPARIN SODIUM:2025-11-19

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HEPARIN SODIUM — approval | AEaH