"45963-611-59" National Drug Code (NDC)

NDC Code	45963-611-59
Package Description	1 VIAL, SINGLE-DOSE in 1 CARTON (45963-611-59) / 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC	45963-611
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Oxaliplatin
Non-Proprietary Name	Oxaliplatin
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20150105
End Marketing Date	20240831
Marketing Category Name	ANDA
Application Number	ANDA078803
Manufacturer	Actavis Pharma, Inc.
Substance Name	OXALIPLATIN
Strength	5
Strength Unit	mg/mL
Pharmacy Classes	Platinum-based Drug [EPC], Platinum-containing Compounds [EXT]