NDC 71288-101 – Oxaliplatin

Oxaliplatin 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC71288-101

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA207325
Marketed since
October 1, 2017
Marketing end
February 28, 2027
Pharmacologic class
Platinum-based Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaliplatin →

Package NDC codes (2)

Package NDCDescriptionSince
71288-101-101 VIAL, SINGLE-DOSE in 1 CARTON (71288-101-10) / 10 mL in 1 VIAL, SINGLE-DOSEOct 1, 2017
71288-101-201 VIAL, SINGLE-DOSE in 1 CARTON (71288-101-20) / 20 mL in 1 VIAL, SINGLE-DOSEOct 1, 2017

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