Orange Book product · Generic (ANDA)
POMALIDOMIDE
POMALIDOMIDE
Generic (ANDA)ANDA 210164TE ABRX APOTEX
At a glance
Jun 11, 2024
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 11, 2024
2 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
POMALIDOMIDE
Strength
1MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 210164
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of POMALIDOMIDE
- 2013POMALYSTBrand (NDA)
NDA 204026 · BRISTOL
- 2024POMALIDOMIDEGeneric (ANDA)
ANDA 210236 · HETERO LABS LTD V
- 2022POMALIDOMIDEGeneric (ANDA)
ANDA 209956 · TEVA PHARMS USA
- 2022POMALIDOMIDEGeneric (ANDA)
ANDA 210275 · MYLAN
- 2020POMALIDOMIDEGeneric (ANDA)
ANDA 210111 · BRECKENRIDGE
- 2020POMALIDOMIDEGeneric (ANDA)
ANDA 210249 · EUGIA PHARMA
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.
