← FDA DRUG APPROVALS

FDA NDA · NDA214410

XOFLUZA

baloxavir marboxil

Sponsor: GENENTECH INC

APPLICATION
NDA214410
TYPE
NDA
ORIGINAL APPROVAL
2020-11-23
LATEST ACTION
2025-05-30
ROUTE
ORAL
DOSAGE FORM
FOR SUSPENSION
MARKETING STATUS
Prescription

Products

XOFLUZA · ReferencePrescription
BALOXAVIR MARBOXIL 30MG/PACKET · FOR SUSPENSION · ORAL
XOFLUZA · ReferencePrescription
BALOXAVIR MARBOXIL 40MG/PACKET · FOR SUSPENSION · ORAL
XOFLUZA · ReferencePrescription
BALOXAVIR MARBOXIL 2MG/ML · FOR SUSPENSION · ORAL

Approval history

2025-05-30Efficacy · Supplement 8 · standardLetterAP
2024-12-19Efficacy · Supplement 7 · standardLetterAP
2024-03-01Efficacy · Supplement 6 · standardLabelAP
2023-06-15Labeling · Supplement 5 · standardLabelAP
2022-08-11Efficacy · Original · standardLabelAP
2021-09-27Labeling · Supplement 1 · standardLetterAP
2020-11-23Type 3 - New Dosage Form · Original · standardLabelAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

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

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →