NDC 61703-363 – Oxaliplatin

Oxaliplatin 5 mg/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC61703-363

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Hospira, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA078813
Marketed since
August 10, 2009
Listing expires
December 31, 2027
Pharmacologic class
Platinum-based Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaliplatin →

Package NDC codes (2)

Package NDCDescriptionSince
61703-363-181 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-18) / 10 mL in 1 VIAL, SINGLE-DOSEAug 10, 2009
61703-363-221 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-22) / 20 mL in 1 VIAL, SINGLE-DOSEAug 10, 2009

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