NDC 63323-193 – Irinotecan Hydrochloride

Irinotecan Hydrochloride 20 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC63323-193

Product details

Brand name
Irinotecan Hydrochloride
Generic name
Irinotecan Hydrochloride
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA077776
Marketed since
April 1, 2009
Listing expires
December 31, 2026
Pharmacologic class
Topoisomerase Inhibitor

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
63323-193-521 VIAL in 1 BOX (63323-193-52) / 2 mL in 1 VIALApr 1, 2009
63323-193-551 VIAL in 1 BOX (63323-193-55) / 5 mL in 1 VIALApr 1, 2009

Recalls mentioning this NDC

Other Irinotecan Hydrochloride products