NDC 50419-488 – Nexavar

Sorafenib 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50419-488

Product details

Brand name
Nexavar
Generic name
Sorafenib
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021923
Marketed since
December 20, 2005
Listing expires
December 31, 2026
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Nexavar →

Package NDC codes (1)

Package NDCDescriptionSince
50419-488-58120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-488-58)Dec 20, 2005

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