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. Author manuscript; available in PMC: 2016 Oct 30.
Published in final edited form as: Future Microbiol. 2015 Oct 30;10(11):1773–1782. doi: 10.2217/fmb.15.106

Table 1.

FDA-approved antiretroviral drugs or drug combinations that target RT

Brand Name Generic Name Approval Date NRTIs Notes
Retrovir zidovudine, azidothymidine, ZDV March 1987 Generic form available
Videx didanosine, dideoxyinosine, ddI October 1991 Generic form available
Hivid zalcitabine, dideoxycytidine, ddC June 1992 No longer marketed due to serious adverse events
Zerit stavudine, d4T June 1994 Use is being phased out due to long-term, irreversible side effects
Epivir lamivudine, 3TC November 1995 Generic form available
Ziagen abacavir sulfate, ABC December 1998
Viread tenofovir disoproxil fumarate, TDF October 2001
Emtriva emtricitabine, (−)-FTC July 2003
NNRTIs
Viramune nevirapine, NVP June 1996
Rescriptor delavirdine, DLV April 1997 Efficacy < NVP and EFV and is not recommended as part of initial therapy. Cross-resistance among the NNRTI class limits DLV use in second-line therapy.
Sustiva efavirenz, EFV September 1998
Intelence etravirine, ETR January 2008
Edurant rilpivirine, RPV May 2011
NRTI combinations
Combivir 3TC+ZDV September 1997
Trizivir ABC+3TC+ZDV November 2000
Epzicom ABC+3TC August 2004
Truvada (−)-FTC+TDF August 2004
NRTI/NNRTI combinations
Atripla (−)-FTC+TDF+EFV July 2006
Complera (−)-FTC+TDF+RPV August 2011