NDC 73555-502 – Revuforj

Revumenib Citrate 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC73555-502

Product details

Brand name
Revuforj
Generic name
revumenib
Labeler
Syndax Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA218944
Marketed since
November 15, 2024
Listing expires
December 31, 2027
Pharmacologic class
Menin Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Revuforj →

Package NDC codes (1)

Package NDCDescriptionSince
73555-502-0030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73555-502-00)Nov 15, 2024

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