NDC 0078-1091 – Scemblix

Asciminib Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0078-1091

Product details

Brand name
Scemblix
Generic name
asciminib
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA215358
Marketed since
October 29, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Scemblix →

Package NDC codes (2)

Package NDCDescriptionSince
0078-1091-2060 TABLET, FILM COATED in 1 BOTTLE (0078-1091-20)Oct 29, 2021
0078-1091-94 sample14 TABLET, FILM COATED in 1 BOTTLE (0078-1091-94)Oct 29, 2021

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