Orange Book product · Brand (NDA)
MUSE
ALPROSTADIL
At a glance
Nov 19, 1996
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 19, 1996
30 yr ago
Today
Pharmaceutical detail
Active ingredient
ALPROSTADIL
Strength
0.125MG
Dosage form
SUPPOSITORY
Route
URETHRAL
TE code
Not listed
Application
NDA 020700
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 2002CAVERJECT IMPULSEBrand (NDA)
NDA 021212 · PFIZER
- 1997CAVERJECTBrand (NDA)
NDA 020755 · PFIZER
- 1997EDEXBrand (NDA)
NDA 020649 · ENDO OPERATIONS
- 1996CAVERJECTBrand (NDA)
NDA 020379 · PFIZER
- —PROSTIN VR PEDIATRICBrand (NDA)
NDA 018484 · PFIZER
- 1999ALPROSTADILGeneric (ANDA)
ANDA 075196 · MEITHEAL
- 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.
