NDC 61703-343 – Mitoxantrone

Mitoxantrone Hydrochloride 2 mg/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug 1 recall

Product NDC61703-343

Product details

Brand name
Mitoxantrone
Generic name
Mitoxantrone
Labeler
Hospira, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA076871
Marketed since
April 11, 2006
Listing expires
December 31, 2026
Pharmacologic class
Topoisomerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for mitoXANTRONE →

Package NDC codes (3)

Package NDCDescriptionSince
61703-343-181 VIAL, MULTI-DOSE in 1 CARTON (61703-343-18) / 10 mL in 1 VIAL, MULTI-DOSEApr 11, 2006
61703-343-651 VIAL, MULTI-DOSE in 1 CARTON (61703-343-65) / 12.5 mL in 1 VIAL, MULTI-DOSEApr 11, 2006
61703-343-661 VIAL, MULTI-DOSE in 1 CARTON (61703-343-66) / 15 mL in 1 VIAL, MULTI-DOSEApr 11, 2006

Recalls mentioning this NDC

Other mitoXANTRONE products