NDC 68083-171 – Oxaliplatin

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

Human Prescription Drug

Product NDC68083-171

Product details

Brand name
Oxaliplatin
Generic name
Oxaliplatin
Labeler
Gland Pharma Limited
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA207385
Marketed since
May 29, 2017
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
68083-171-0120 mL in 1 VIAL (68083-171-01)May 29, 2017

Other Oxaliplatin products