NDC 0143-9701 – Irinotecan Hydrochloride

Irinotecan Hydrochloride 20 mg/mL · Injection · Intravenous

Human Prescription Drug 3 recalls

Product NDC0143-9701

Product details

Brand name
Irinotecan Hydrochloride
Generic name
Irinotecan Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA091032
Marketed since
December 20, 2010
Listing expires
December 31, 2026
Pharmacologic class
Topoisomerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Irinotecan Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9701-015 mL in 1 VIAL, GLASS (0143-9701-01)Dec 20, 2010

Recalls mentioning this NDC

Other Irinotecan Hydrochloride products