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approval · primary record

CYCLOSPORINE

FDA · NDA · 2025-08-21

AgencyFDA
Submission typeNDA
Action date2025-08-21
BrandRESTASIS MULTIDOSE
SponsorABBVIE
RouteOPHTHALMIC

Provenance

  • Source: openFDA Drugs@FDA
  • Fetched at: 2026-10-28T02:35:32.063Z
  • Licence class: public-domain
  • Verdict: primary-source
  • Entity id: FDA:CYCLOSPORINE:2025-08-21

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CYCLOSPORINE — approval | AEaH