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FDA NDA · NDA218709

XOLREMDI

mavorixafor

Sponsor: X4 PHARMS

APPLICATION
NDA218709
TYPE
NDA
ORIGINAL APPROVAL
2024-04-26
LATEST ACTION
2024-04-26
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Prescription

Products

XOLREMDI · ReferencePrescription
MAVORIXAFOR 100MG · CAPSULE · ORAL

Approval history

2024-04-26Type 1 - New Molecular Entity · Original · priorityLabelAP
VIEW ON DRUGS@FDA ↗

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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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