Iclusig

Product NDC
76189-533
11-digit product format
761890533
Labeler code
76189
Product ID
76189-533_618b6b2f-ca86-4839-9170-e873e279d592
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ponatinib hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ARIAD Pharmaceuticals, Inc.
Application
NDA203469
Marketing category
NDA
Marketing start
2015-04-22
Marketing end
2020-07-26
Substance
PONATINIB HYDROCHLORIDE
Active strength
30 mg/1
Pharmacologic classes
Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record