← FDA DRUG APPROVALS
FDA NDA · NDA021752
TRUVADA
emtricitabine and tenofovir disoproxil fumarate
Sponsor: GILEAD
APPLICATION
NDA021752
TYPE
NDA
ORIGINAL APPROVAL
2004-08-02
LATEST ACTION
2024-04-29
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription
Products
TRUVADA · ReferencePrescription
EMTRICITABINE 167MG, TENOFOVIR DISOPROXIL FUMARATE 250MG · TABLET · ORAL
TRUVADA · ReferencePrescription
EMTRICITABINE 100MG, TENOFOVIR DISOPROXIL FUMARATE 150MG · TABLET · ORAL
TRUVADA · ReferencePrescription
EMTRICITABINE 133MG, TENOFOVIR DISOPROXIL FUMARATE 200MG · TABLET · ORAL
TRUVADA · ReferencePrescription
EMTRICITABINE 200MG, TENOFOVIR DISOPROXIL FUMARATE 300MG · TABLET · ORAL
Approval history
2017-12-08REMS · Supplement 54AP
2014-07-11Manufacturing (CMC) · Supplement 45 · priorityAP
2013-11-27Manufacturing (CMC) · Supplement 33 · priorityAP
2013-11-08Manufacturing (CMC) · Supplement 40 · priorityAP
2013-08-21Manufacturing (CMC) · Supplement 38 · priorityAP
2013-08-15Manufacturing (CMC) · Supplement 37 · priorityAP
2013-07-08Manufacturing (CMC) · Supplement 39 · priorityAP
2013-06-17Manufacturing (CMC) · Supplement 36 · priorityAP
2010-01-15Manufacturing (CMC) · Supplement 21 · priorityAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
Weekly Briefing
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.