NDC 57894-640 – Tremfya

Guselkumab 100 mg/mL · Injection · Subcutaneous

Human Prescription Drug 1 recall

Product NDC57894-640

Product details

Brand name
Tremfya
Generic name
Guselkumab
Labeler
Janssen Biotech, Inc.
Dosage form
Injection
Route
Subcutaneous
Marketing category
BLA · BLA761061
Marketed since
July 13, 2017
Listing expires
December 31, 2027
Pharmacologic class
Interleukin-23 Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Tremfya →

Package NDC codes (5)

Package NDCDescriptionSince
57894-640-011 SYRINGE in 1 CARTON (57894-640-01) / 1 mL in 1 SYRINGEJul 13, 2017
57894-640-041 SYRINGE in 1 CARTON (57894-640-04) / 1 mL in 1 SYRINGEJul 13, 2017
57894-640-061 SYRINGE in 1 CARTON (57894-640-06) / 1 mL in 1 SYRINGE (57894-640-03)Mar 25, 2025
57894-640-111 SYRINGE in 1 CARTON (57894-640-11) / 1 mL in 1 SYRINGEJan 28, 2019
57894-640-991 SYRINGE in 1 CARTON (57894-640-99) / 1 mL in 1 SYRINGEJan 28, 2019

Recalls mentioning this NDC

Other Tremfya products