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General MedicationsORALStandard

KOSELUGO

SELUMETINIB SULFATE

Standard Dose
EQ 7.5MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview KOSELUGO is listed in Drugs@FDA under application 219943 (NDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient SELUMETINIB SULFATE Form and strength GRANULE;ORAL - EQ 7.5MG BASE Sponsor ASTRAZENECA Submission history Latest submission status date: 2025-11-19 00:00:00.

Structured Monograph

Clinical summary

Approval overview KOSELUGO is listed in Drugs@FDA under application 219943 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient SELUMETINIB SULFATE Form and strength GRANULE;ORAL - EQ 7.5MG BASE Sponsor ASTRAZENECA Submission history Latest submission status date: 2025-11-19 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.