NDC 31722-358 – Oxaliplatin

Oxaliplatin 100 mg/20mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC31722-358

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA217925
Marketed since
January 27, 2025
Listing expires
December 31, 2026
Pharmacologic class
Platinum-based Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaliplatin →

Package NDC codes (1)

Package NDCDescriptionSince
31722-358-201 VIAL, SINGLE-DOSE in 1 CARTON (31722-358-20) / 20 mL in 1 VIAL, SINGLE-DOSEJan 27, 2025

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