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Pronunciation | /ˌɛmtrəˈsaɪtəbiːn/ EM-trə-SY-tə-been |
Trade names | Emtriva |
Other names | FTC |
AHFS/Drugs.com | Monograph |
MedlinePlus | a604004 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | 93% |
Protein binding | Very low (less than 4%) |
Metabolism | Hepatic oxidation and glucuronidation CYP system not involved |
Elimination half-life | 10 hours |
Excretion | Renal (86%) and fecal (14%) |
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ECHA InfoCard | 100.120.945 |
Chemical and physical data | |
Formula | C8H10FN3O3S |
Molar mass | 247.24 g·mol−1 |
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Emtricitabine (commonly called FTC, systematic name 2',3'-dideoxy-5-fluoro-3'-thiacytidine[2]), with trade name Emtriva (formerly Coviracil), is a nucleoside reverse-transcriptase inhibitor (NRTI) for the prevention and treatment of HIV infection in adults and children. In 2019, it was the 494th most commonly prescribed medication in the United States, with more than 3 thousand prescriptions.[3]
Emtricitabine makes up one fourth of the Quad pill (brand names: Stribild and Genvoya). It is also marketed in a fixed-dose combination with tenofovir disoproxil (Viread) under the brand name Truvada, and with tenofovir alafenamide (Vemlidy) under the brand name Descovy. In fixed-dose combinations with tenofovir or with efavirenz and tenofovir it is on the World Health Organization's List of Essential Medicines.[4] A fixed-dose triple combination of emtricitabine, tenofovir and efavirenz (Sustiva, marketed by Bristol-Myers Squibb) was approved by the U.S. Food and Drug Administration (FDA) on July 12, 2006, under the brand name Atripla.