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General MedicationsSUBCUTANEOUSStandard

ZILBRYSQ

ZILUCOPLAN SODIUM

Standard Dose
EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML)
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview ZILBRYSQ is listed in Drugs@FDA under application 216834 (NDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient ZILUCOPLAN SODIUM Form and strength SOLUTION;SUBCUTANEOUS - EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML) Sponsor UCB INC Submission history Latest submission status date: 2026-01-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview ZILBRYSQ is listed in Drugs@FDA under application 216834 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient ZILUCOPLAN SODIUM Form and strength SOLUTION;SUBCUTANEOUS - EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML) Sponsor UCB INC Submission history Latest submission status date: 2026-01-22 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.