63020-533-30 |
63020-533 |
HUMAN PRESCRIPTION DRUG |
Iclusig |
ponatinib hydrochloride |
TABLET, FILM COATED |
ORAL |
20150422 |
N/A |
NDA |
NDA203469 |
Takeda Pharmaceuticals America, Inc. |
PONATINIB HYDROCHLORIDE |
30 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63020-533-30) |
63020-534-30 |
63020-534 |
HUMAN PRESCRIPTION DRUG |
Iclusig |
ponatinib hydrochloride |
TABLET, FILM COATED |
ORAL |
20121214 |
N/A |
NDA |
NDA203469 |
Takeda Pharmaceuticals America, Inc. |
PONATINIB HYDROCHLORIDE |
45 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63020-534-30) |
63020-535-30 |
63020-535 |
HUMAN PRESCRIPTION DRUG |
Iclusig |
ponatinib hydrochloride |
TABLET, FILM COATED |
ORAL |
20121214 |
N/A |
NDA |
NDA203469 |
Takeda Pharmaceuticals America, Inc. |
PONATINIB HYDROCHLORIDE |
15 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63020-535-30) |
63020-535-60 |
63020-535 |
HUMAN PRESCRIPTION DRUG |
Iclusig |
ponatinib hydrochloride |
TABLET, FILM COATED |
ORAL |
20121214 |
N/A |
NDA |
NDA203469 |
Takeda Pharmaceuticals America, Inc. |
PONATINIB HYDROCHLORIDE |
15 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (63020-535-60) |
63020-536-30 |
63020-536 |
HUMAN PRESCRIPTION DRUG |
Iclusig |
ponatinib hydrochloride |
TABLET, FILM COATED |
ORAL |
20210111 |
N/A |
NDA |
NDA203469 |
Takeda Pharmaceuticals America, Inc. |
PONATINIB HYDROCHLORIDE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63020-536-30) |