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

BONIVA

IBANDRONATE SODIUM

Standard Dose
EQ 3MG BASE/3ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview BONIVA is listed in Drugs@FDA under application 021858 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient IBANDRONATE SODIUM Form and strength INJECTABLE;INTRAVENOUS - EQ 3MG BASE/3ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ROCHE Submission history Latest submission status date: 2022-01-11 00:00:00.

Structured Monograph

Clinical summary

Approval overview BONIVA is listed in Drugs@FDA under application 021858 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient IBANDRONATE SODIUM Form and strength INJECTABLE;INTRAVENOUS - EQ 3MG BASE/3ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ROCHE Submission history Latest submission status date: 2022-01-11 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.