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General MedicationsIMPLANTATIONStandard

SINUVA

MOMETASONE FUROATE

Standard Dose
1.35MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview SINUVA is listed in Drugs@FDA under application 209310 (NDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient MOMETASONE FUROATE Form and strength IMPLANT;IMPLANTATION - 1.35MG Sponsor INTERSECT ENT INC Submission history Latest submission status date: 2023-01-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview SINUVA is listed in Drugs@FDA under application 209310 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient MOMETASONE FUROATE Form and strength IMPLANT;IMPLANTATION - 1.35MG Sponsor INTERSECT ENT INC Submission history Latest submission status date: 2023-01-20 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.