Iclusig - 76189-534-90 - (ponatinib hydrochloride)

Alphabetical Index


Drug Information of Iclusig

Product NDC: 76189-534
Proprietary Name: Iclusig
Non Proprietary Name: ponatinib hydrochloride
Active Ingredient(s): 45    mg/1 & nbsp;   ponatinib hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Iclusig

Product NDC: 76189-534
Labeler Name: ARIAD Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA203469
Marketing Category: NDA
Start Marketing Date: 20121214

Package Information of Iclusig

Package NDC: 76189-534-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (76189-534-90)

NDC Information of Iclusig

NDC Code 76189-534-90
Proprietary Name Iclusig
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (76189-534-90)
Product NDC 76189-534
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ponatinib hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121214
Marketing Category Name NDA
Labeler Name ARIAD Pharmaceuticals, Inc.
Substance Name PONATINIB HYDROCHLORIDE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Iclusig


General Information