NDC 72893-007 – Zevalin

· Kit

Human Prescription Drug

Product NDC72893-007

Product details

Brand name
Zevalin
Generic name
Ibritumomab tiuxetan
Labeler
Acrotech Biopharma Inc
Dosage form
Kit
Marketing category
BLA · BLA125019
Marketed since
February 19, 2002
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Zevalin →

    Package NDC codes (1)

    Package NDCDescriptionSince
    72893-007-041 KIT in 1 CARTON (72893-007-04) * 10 mL in 1 VIAL * 2 mL in 1 VIAL * 2 mL in 1 VIALFeb 19, 2002