NDC 69448-019 – Imuldosa

Ustekinumab-srlf 130 mg/26mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC69448-019

Product details

Brand name
Imuldosa
Generic name
Ustekinumab-srlf
Labeler
Accord BioPharma Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
BLA · BLA761364
Marketed since
October 18, 2024
Listing expires
December 31, 2027
Pharmacologic class
Interleukin-12 Antagonist; Interleukin-23 Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Imuldosa →

Package NDC codes (1)

Package NDCDescriptionSince
69448-019-261 VIAL, SINGLE-USE in 1 CARTON (69448-019-26) / 26 mL in 1 VIAL, SINGLE-USEOct 18, 2024

Recalls mentioning this NDC

Other Imuldosa products