LAMIVUDINE/NEVIRAPINE/ZIDOVUDINE TABLETS
Pre-Launchlamivudine; nevirapine; zidovudine
NDAORALTABLET, FOR SUSPENSIONPriority Review
Lifecycle
Pre-Launch
Data completeness
2/8 — Basic
Priority Review
LAMIVUDINE/NEVIRAPINE/ZIDOVUDINE TABLETS (lamivudine; nevirapine; zidovudine) by Matrix Surgical USA is fixed-dose combination of the hiv‑1 antiretroviral agents abacavir, dolutegravir, and lamivudine [see microbiology ()]. Approved for hiv-1 infection in adults, weighing at least 6 kg.
Drug data last refreshed Yesterday · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
This is a fixed-dose combination oral tablet containing lamivudine, nevirapine, and zidovudine for the treatment of HIV-1 infection in adults and pediatric patients weighing at least 6 kg. The combination works by inhibiting HIV-1 reverse transcriptase through multiple mechanisms (nucleoside and non-nucleoside inhibition). This triple-agent regimen represents a foundational antiretroviral therapy approach.
Pre-Launch
Pre-launch stage indicates opportunity for launch readiness teams, but significant competitive pressure from multiple generic entrants may limit commercial upside and long-term team expansion.
Mechanism of Action
fixed-dose combination of the HIV‑1 antiretroviral agents abacavir, dolutegravir, and lamivudine [see Microbiology ()].
Indications (2)
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.