CISplatin - 44567-509-01 - (CISplatin)

Alphabetical Index


Drug Information of CISplatin

Product NDC: 44567-509
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: 44567-509
Labeler Name: WG Critical Care, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018057
Marketing Category: NDA
Start Marketing Date: 20120113

Package Information of CISplatin

Package NDC: 44567-509-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (44567-509-01) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of CISplatin

NDC Code 44567-509-01
Proprietary Name CISplatin
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (44567-509-01) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 44567-509
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CISplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120113
Marketing Category Name NDA
Labeler Name WG Critical Care, LLC
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