Orange Book product · Generic (ANDA)
ALPROSTADIL
ALPROSTADIL
Generic (ANDA)ANDA 074815TE APRX HIKMA
At a glance
Jan 20, 1998
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 20, 1998
28 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
ALPROSTADIL
Strength
0.5MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 074815
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ALPROSTADIL
- 2002CAVERJECT IMPULSEBrand (NDA)
NDA 021212 · PFIZER
- 1997CAVERJECTBrand (NDA)
NDA 020755 · PFIZER
- 1997EDEXBrand (NDA)
NDA 020649 · ENDO OPERATIONS
- 1996MUSEBrand (NDA)
NDA 020700 · VIATRIS
- 1996CAVERJECTBrand (NDA)
NDA 020379 · PFIZER
- —PROSTIN VR PEDIATRICBrand (NDA)
NDA 018484 · PFIZER
- 1999ALPROSTADILGeneric (ANDA)
ANDA 075196 · MEITHEAL
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.
