NDC 57894-651 – Tremfya

Guselkumab 200 mg/2mL · Injection · Subcutaneous

Human Prescription Drug 1 recall

Product NDC57894-651

Product details

Brand name
Tremfya
Generic name
Guselkumab
Labeler
Janssen Biotech, Inc.
Dosage form
Injection
Route
Subcutaneous
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 (4)

Package NDCDescriptionSince
57894-651-021 SYRINGE in 1 CARTON (57894-651-02) / 2 mL in 1 SYRINGE (57894-651-01)Sep 11, 2024
57894-651-042 CARTON in 1 CARTON (57894-651-04) / 1 SYRINGE in 1 CARTON (57894-651-02) / 2 mL in 1 SYRINGE (57894-651-01)Mar 20, 2025
57894-651-221 SYRINGE in 1 CARTON (57894-651-22) / 2 mL in 1 SYRINGE (57894-651-11)Sep 11, 2024
57894-651-921 SYRINGE in 1 CARTON (57894-651-92) / 2 mL in 1 SYRINGE (57894-651-99)Sep 11, 2024

Recalls mentioning this NDC

Other Tremfya products