NDC 67184-0502 – Oxaliplatin

Oxaliplatin 100 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC67184-0502

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA204616
Marketed since
May 11, 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
67184-0502-11 VIAL, SINGLE-DOSE in 1 CARTON (67184-0502-1) / 20 mL in 1 VIAL, SINGLE-DOSEMay 11, 2016

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