Emtricitabine/rilpivirine/tenofovir
              < Emtricitabine < rilpivirine 
 
            
          
| Combination of | |
|---|---|
| Emtricitabine | Nucleoside analog reverse-transcriptase inhibitor | 
| Rilpivirine | Non-nucleoside reverse transcriptase inhibitor | 
| Tenofovir disoproxil | Nucleotide analog reverse-transcriptase inhibitor | 
| Clinical data | |
| Trade names | Complera, Eviplera | 
| AHFS/Drugs.com | Multum Consumer Information | 
| MedlinePlus | a616021 | 
| License data | |
| Pregnancy category | 
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| Routes of administration | By mouth | 
| ATC code | |
| Legal status | |
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| ChemSpider | 
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Emtricitabine/rilpivirine/tenofovir, sold under the brand name Complera among others, is a fixed-dose combination of antiretroviral drugs for the treatment of HIV/AIDS. The drug was co-developed by Gilead Sciences and Johnson & Johnson's Tibotec division and was approved by the US Food and Drug Administration (FDA) in August 2011, and by the European Medicines Agency in November 2011, for patients who have not previously been treated for HIV. It is available as a once-a-day single tablet.
In the European Union it is marketed as Eviplera and in the US as Complera.