NDC 72266-162 – Oxaliplatin

Oxaliplatin 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC72266-162

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
FOSUN PHARMA USA INC.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA207325
Marketed since
March 30, 2020
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
72266-162-011 VIAL, SINGLE-USE in 1 CARTON (72266-162-01) / 20 mL in 1 VIAL, SINGLE-USEMar 30, 2020

Other Oxaliplatin products