EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE
Post-LOEefavirenz, emtricitabine and tenofovir disoproxil fumarate
ANDAORALTABLET
Approved
Nov 2018
Lifecycle
Post-LOE
Competitive Pressure
30/100
Data completeness
3/8 — Basic
EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE (efavirenz, emtricitabine and tenofovir disoproxil fumarate) by Teva is non-nucleoside reverse transcriptase inhibitors [moa]. Approved for human immunodeficiency virus 1 non-nucleoside analog reverse transcriptase inhibitor [epc]. First approved in 2018.
Drug data last refreshed 18h ago
Mechanism of Action
Non-Nucleoside Reverse Transcriptase Inhibitors
Pharmacologic Class:
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Company
Teva
Israel - Petach Tikva
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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.