← FDA DRUG APPROVALS
FDA NDA · NDA210251
BIKTARVY
bictegravir sodium, emtricitabine, and tenofovir alafenamide fumarate
Sponsor: GILEAD SCIENCES INC
APPLICATION
NDA210251
TYPE
NDA
ORIGINAL APPROVAL
2018-02-07
LATEST ACTION
2026-05-21
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription
Products
BIKTARVY · ReferencePrescription
BICTEGRAVIR SODIUM EQ 50MG BASE, EMTRICITABINE 200MG, TENOFOVIR ALAFENAMIDE FUMARATE EQ 25MG BASE · TABLET · ORAL
BIKTARVY · ReferencePrescription
BICTEGRAVIR SODIUM EQ 30MG BASE, EMTRICITABINE 120MG, TENOFOVIR ALAFENAMIDE FUMARATE EQ 15MG BASE · TABLET · ORAL
Approval history
2018-02-07Type 1 - New Molecular Entity and Type 4 - New Combination · Original · priority — Label ↗AP
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.
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