NDC 68001-705 – Paclitaxel

Paclitaxel 6 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC68001-705

Product details

Brand name
Paclitaxel
Generic name
Paclitaxel
Labeler
BluePoint Laboratories
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA216874
Marketed since
April 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Microtubule Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Paclitaxel →

Package NDC codes (1)

Package NDCDescriptionSince
68001-705-271 VIAL, MULTI-DOSE in 1 CARTON (68001-705-27) / 50 mL in 1 VIAL, MULTI-DOSEApr 9, 2026

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