NDC 57894-080 – Lazcluze

Lazertinib 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC57894-080

Product details

Brand name
Lazcluze
Generic name
Lazertinib
Labeler
Janssen Biotech, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA219008
Marketed since
August 20, 2024
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lazcluze →

Package NDC codes (2)

Package NDCDescriptionSince
57894-080-601 BOTTLE in 1 CARTON (57894-080-60) / 60 TABLET, FILM COATED in 1 BOTTLEAug 20, 2024
57894-080-901 BOTTLE in 1 CARTON (57894-080-90) / 90 TABLET, FILM COATED in 1 BOTTLEAug 20, 2024

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