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General MedicationsORALGeneric

TRIZIVIR

ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE

Standard Dose
EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 TRIZIVIR is listed in Drugs@FDA under application 021205 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE Form and strength TABLET;ORAL - EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VIIV HLTHCARE Submission history Latest submission status date: 2021-02-17 00:00:00.

Structured Monograph

Clinical summary

Approval overview TRIZIVIR is listed in Drugs@FDA under application 021205 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE Form and strength TABLET;ORAL - EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VIIV HLTHCARE Submission history Latest submission status date: 2021-02-17 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.