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strength TABLET;ORAL - EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VIIV HLTHCARE Submission history Latest submission status date: 2021-02-17 00:00:00.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strength TABLET;ORAL - EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VIIV HLTHCARE Submission history Latest submission status date: 2021-02-17 00:00:00.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