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General MedicationsORALStandard

ROZLYTREK

ENTRECTINIB

Standard Dose
50MG/PACKET
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Prescription
Summary

Approval overview ROZLYTREK is listed in Drugs@FDA under application 218550 (NDA).

Review priority: PRIORITY Marketing status: Prescription Active ingredient ENTRECTINIB Form and strength PELLETS;ORAL - 50MG/PACKET Sponsor GENENTECH INC Submission history Latest submission status date: 2023-10-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview ROZLYTREK is listed in Drugs@FDA under application 218550 (NDA). Review priority: PRIORITY Marketing status: Prescription Active ingredient ENTRECTINIB Form and strength PELLETS;ORAL - 50MG/PACKET Sponsor GENENTECH INC Submission history Latest submission status date: 2023-10-20 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: PRIORITY

Interaction Notes

  • No interaction notes stored yet.