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General MedicationsORALGeneric

VORTIOXETINE HYDROBROMIDE

VORTIOXETINE HYDROBROMIDE

Standard Dose
EQ 5MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview VORTIOXETINE HYDROBROMIDE is listed in Drugs@FDA under application 211146 (ANDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient VORTIOXETINE HYDROBROMIDE Form and strength TABLET;ORAL - EQ 5MG BASE Sponsor ZYDUS PHARMS Submission history Latest submission status date: 2024-04-02 00:00:00.

Structured Monograph

Clinical summary

Approval overview VORTIOXETINE HYDROBROMIDE is listed in Drugs@FDA under application 211146 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient VORTIOXETINE HYDROBROMIDE Form and strength TABLET;ORAL - EQ 5MG BASE Sponsor ZYDUS PHARMS Submission history Latest submission status date: 2024-04-02 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.