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FDA NDA · NDA220436

NAVITRUX

fosaprepitant

Sponsor: AVYXA HOLDINGS

APPLICATION
NDA220436
TYPE
NDA
ORIGINAL APPROVAL
2026-06-24
LATEST ACTION
2026-06-24
ROUTE
INTRAVENOUS
DOSAGE FORM
POWDER
MARKETING STATUS
Prescription

Products

NAVITRUX · ReferencePrescription
FOSAPREPITANT DIMEGLUMINE EQ 150MG BASE/VIAL · POWDER · INTRAVENOUS

Approval history

2026-06-24Type 5 - New Formulation or New Manufacturer · Original · standardLetterAP
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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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