NDC 0781-3531 – Paclitaxel

Paclitaxel 100 mg/20mL · Injection, Powder, Lyophilized, For Suspension · Intravenous

Human Prescription Drug

Product NDC0781-3531

Product details

Brand name
Paclitaxel
Generic name
Paclitaxel
Labeler
Sandoz Inc
Dosage form
Injection, Powder, Lyophilized, For Suspension
Route
Intravenous
Marketing category
ANDA · ANDA212700
Marketed since
October 8, 2024
Listing expires
December 31, 2026
Pharmacologic class
Microtubule Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paclitaxel →

Package NDC codes (1)

Package NDCDescriptionSince
0781-3531-911 VIAL, SINGLE-DOSE in 1 CARTON (0781-3531-91) / 20 mL in 1 VIAL, SINGLE-DOSEOct 9, 2024

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