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approval · primary record

PALIPERIDONE PALMITATE

FDA · NDA · 2025-01-22

AgencyFDA
Submission typeNDA
Action date2025-01-22
BrandERZOFRI
SponsorLUYE INNOMIND PHARMA
RouteINTRAMUSCULAR

Provenance

  • Source: openFDA Drugs@FDA
  • Fetched at: 2026-10-28T03:30:02.628Z
  • Licence class: public-domain
  • Verdict: primary-source
  • Entity id: FDA:PALIPERIDONE PALMITATE:2025-01-22

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PALIPERIDONE PALMITATE — approval | AEaH