Orange Book product · Generic (ANDA)
ALPROSTADIL
ALPROSTADIL
Generic (ANDA)ANDA 075196TE APRX MEITHEAL
At a glance
Apr 30, 1999
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 30, 1999
27 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
ALPROSTADIL
Strength
0.5MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 075196
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
- 1998ALPROSTADILGeneric (ANDA)
ANDA 074815 · HIKMA
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.
