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General MedicationsSUBCUTANEOUSStandard

PROLIA

DENOSUMAB

Standard Dose
60MG/ML
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview PROLIA is listed in Drugs@FDA under application 125320 (BLA).

Review priority: STANDARD Marketing status: Prescription Active ingredient DENOSUMAB Form and strength INJECTABLE; SUBCUTANEOUS - 60MG/ML Sponsor AMGEN Submission history Latest submission status date: 2025-05-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview PROLIA is listed in Drugs@FDA under application 125320 (BLA). Review priority: STANDARD Marketing status: Prescription Active ingredient DENOSUMAB Form and strength INJECTABLE; SUBCUTANEOUS - 60MG/ML Sponsor AMGEN Submission history Latest submission status date: 2025-05-30 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.