Cisplatin - 55390-112-50 - (Cisplatin)

Alphabetical Index


Drug Information of Cisplatin

Product NDC: 55390-112
Proprietary Name: Cisplatin
Non Proprietary Name: Cisplatin
Active Ingredient(s): 1    mg/mL & nbsp;   Cisplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cisplatin

Product NDC: 55390-112
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075036
Marketing Category: ANDA
Start Marketing Date: 20010115

Package Information of Cisplatin

Package NDC: 55390-112-50
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (55390-112-50) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of Cisplatin

NDC Code 55390-112-50
Proprietary Name Cisplatin
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (55390-112-50) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 55390-112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cisplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20010115
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name CISPLATIN
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of Cisplatin


General Information