NDC 67184-0510 – Oxaliplatin

Oxaliplatin 200 mg/40mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC67184-0510

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA204368
Marketed since
June 7, 2016
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
67184-0510-11 VIAL, SINGLE-USE in 1 CARTON (67184-0510-1) / 40 mL in 1 VIAL, SINGLE-USEJun 7, 2016

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