NDC 63323-763 – Paclitaxel

Paclitaxel 6 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC63323-763

Product details

Brand name
Paclitaxel
Generic name
Paclitaxel
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA077574
Marketed since
March 20, 2009
Listing expires
December 31, 2026
Pharmacologic class
Microtubule Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paclitaxel →

Package NDC codes (2)

Package NDCDescriptionSince
63323-763-161 VIAL, MULTI-DOSE in 1 CARTON (63323-763-16) / 16.7 mL in 1 VIAL, MULTI-DOSEMar 20, 2009
63323-763-501 VIAL, MULTI-DOSE in 1 CARTON (63323-763-50) / 50 mL in 1 VIAL, MULTI-DOSEMar 20, 2009

Recalls mentioning this NDC

Other Paclitaxel products