Orange Book product · Generic (ANDA)
EPOPROSTENOL SODIUM
EPOPROSTENOL SODIUM
Generic (ANDA)ANDA 210473TE AP2RX SUN PHARM
At a glance
Jan 15, 2021
Approved
Generic (ANDA)
Application
AP2
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 15, 2021
5 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
EPOPROSTENOL SODIUM
Strength
EQ 0.5MG BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP2
Application
ANDA 210473
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of EPOPROSTENOL SODIUM
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.
