NDC 58468-0251 – Wayrilz

Rilzabrutinib 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC58468-0251

Product details

Brand name
Wayrilz
Generic name
Rilzabrutinib
Labeler
Genzyme Corporation
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA219685
Marketed since
August 29, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Wayrilz →

Package NDC codes (2)

Package NDCDescriptionSince
58468-0251-52 BLISTER PACK in 1 CARTON (58468-0251-5) / 28 TABLET, FILM COATED in 1 BLISTER PACK (58468-0251-0)Aug 29, 2025
58468-0251-61 BOTTLE in 1 CARTON (58468-0251-6) / 60 TABLET, FILM COATED in 1 BOTTLEAug 29, 2025