Cisplatin - 0069-0081-01 - (Cisplatin)

Alphabetical Index


Drug Information of Cisplatin

Product NDC: 0069-0081
Proprietary Name: Cisplatin
Non Proprietary Name: Cisplatin
Active Ingredient(s): 1    mg/mL & nbsp;   Cisplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cisplatin

Product NDC: 0069-0081
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091062
Marketing Category: ANDA
Start Marketing Date: 20120419

Package Information of Cisplatin

Package NDC: 0069-0081-01
Package Description: 100 mL in 1 VIAL (0069-0081-01)

NDC Information of Cisplatin

NDC Code 0069-0081-01
Proprietary Name Cisplatin
Package Description 100 mL in 1 VIAL (0069-0081-01)
Product NDC 0069-0081
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cisplatin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20120419
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer Inc.
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