NDC 16729-332 – Oxaliplatin

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

Human Prescription Drug

Product NDC16729-332

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Accord Healthcare Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA207474
Marketed since
May 17, 2018
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
16729-332-031 VIAL, SINGLE-DOSE in 1 CARTON (16729-332-03) / 10 mL in 1 VIAL, SINGLE-DOSEMay 17, 2018
16729-332-051 VIAL, SINGLE-DOSE in 1 CARTON (16729-332-05) / 20 mL in 1 VIAL, SINGLE-DOSEMay 17, 2018

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