Skip to main content
MedicHelpLine
Join Free
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsINTRAVENOUSStandard

ZEVTERA

CEFTOBIPROLE MEDOCARIL SODIUM

Standard Dose
667MG/VIAL
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Prescription
Summary

Approval overview ZEVTERA is listed in Drugs@FDA under application 218275 (NDA).

Review priority: PRIORITY Marketing status: Prescription Active ingredient CEFTOBIPROLE MEDOCARIL SODIUM Form and strength POWDER;INTRAVENOUS - 667MG/VIAL Sponsor ISTX Submission history Latest submission status date: 2024-04-03 00:00:00.

Structured Monograph

Clinical summary

Approval overview ZEVTERA is listed in Drugs@FDA under application 218275 (NDA). Review priority: PRIORITY Marketing status: Prescription Active ingredient CEFTOBIPROLE MEDOCARIL SODIUM Form and strength POWDER;INTRAVENOUS - 667MG/VIAL Sponsor ISTX Submission history Latest submission status date: 2024-04-03 00:00:00. Submission type: ORIG.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.