NDC 57894-650 – Tremfya

Guselkumab 200 mg/20mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC57894-650

Product details

Brand name
Tremfya
Generic name
Guselkumab
Labeler
Janssen Biotech, Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
BLA · BLA761061
Marketed since
September 11, 2024
Listing expires
December 31, 2027
Pharmacologic class
Interleukin-23 Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Tremfya →

Package NDC codes (1)

Package NDCDescriptionSince
57894-650-021 VIAL, SINGLE-DOSE in 1 CARTON (57894-650-02) / 20 mL in 1 VIAL, SINGLE-DOSE (57894-650-01)Sep 11, 2024

Recalls mentioning this NDC

Other Tremfya products