NDC 50742-402 – Irinotecan Hydrochloride

Irinotecan Hydrochloride 100 mg/5mL · Injection · Intravenous

Human Prescription Drug 2 recalls

Product NDC50742-402

Product details

Brand name
Irinotecan Hydrochloride
Generic name
Irinotecan Hydrochloride
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA206935
Marketed since
June 5, 2017
Marketing end
September 30, 2026
Pharmacologic class
Topoisomerase Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50742-402-051 VIAL, GLASS in 1 CARTON (50742-402-05) / 5 mL in 1 VIAL, GLASSJun 5, 2017

Recalls mentioning this NDC

Other Irinotecan Hydrochloride products