NDC 71288-172 – Oxaliplatin

Oxaliplatin 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC71288-172

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA217348
Marketed since
January 11, 2024
Listing expires
December 31, 2026
Pharmacologic class
Platinum-based Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaliplatin →

Package NDC codes (2)

Package NDCDescriptionSince
71288-172-211 VIAL, SINGLE-DOSE in 1 CARTON (71288-172-21) / 20 mL in 1 VIAL, SINGLE-DOSEJan 11, 2024
71288-172-921 VIAL, SINGLE-DOSE in 1 CARTON (71288-172-92) / 20 mL in 1 VIAL, SINGLE-DOSEJan 11, 2024

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