NDC 66733-948 – Erbitux

Cetuximab 2 mg/mL · Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC66733-948

Product details

Brand name
Erbitux
Generic name
Cetuximab
Labeler
ImClone LLC
Dosage form
Solution
Route
Intravenous
Marketing category
BLA · BLA125084
Marketed since
February 12, 2004
Listing expires
December 31, 2027
Pharmacologic class
Epidermal Growth Factor Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Erbitux →

Package NDC codes (1)

Package NDCDescriptionSince
66733-948-231 VIAL, SINGLE-DOSE in 1 CARTON (66733-948-23) / 50 mL in 1 VIAL, SINGLE-DOSEFeb 12, 2004

Recalls mentioning this NDC

Other Erbitux products