Orange Book product · Generic (ANDA)
NILOTINIB HYDROCHLORIDE
NILOTINIB HYDROCHLORIDE
Generic (ANDA)ANDA 203640TE ABRX APOTEX
At a glance
Jan 05, 2024
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 05, 2024
2 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
NILOTINIB HYDROCHLORIDE
Strength
EQ 50MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 203640
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NILOTINIB HYDROCHLORIDE
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
