Zytiga - 57894-150-12 - (abiraterone acetate)

Alphabetical Index


Drug Information of Zytiga

Product NDC: 57894-150
Proprietary Name: Zytiga
Non Proprietary Name: abiraterone acetate
Active Ingredient(s): 250    mg/1 & nbsp;   abiraterone acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zytiga

Product NDC: 57894-150
Labeler Name: Janssen Biotech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202379
Marketing Category: NDA
Start Marketing Date: 20110428

Package Information of Zytiga

Package NDC: 57894-150-12
Package Description: 120 TABLET in 1 BOTTLE (57894-150-12)

NDC Information of Zytiga

NDC Code 57894-150-12
Proprietary Name Zytiga
Package Description 120 TABLET in 1 BOTTLE (57894-150-12)
Product NDC 57894-150
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name abiraterone acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110428
Marketing Category Name NDA
Labeler Name Janssen Biotech, Inc.
Substance Name ABIRATERONE ACETATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cytochrome P450 17A1 Inhibitors [MoA],Cytochrome P450 17A1 Inhibitor [EPC]

Complete Information of Zytiga


General Information