Orange Book product · Generic (ANDA)
ALCLOMETASONE DIPROPIONATE
ALCLOMETASONE DIPROPIONATE
At a glance
Jul 12, 2005
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 12, 2005
21 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
ALCLOMETASONE DIPROPIONATE
Strength
0.05%
Dosage form
CREAM
Route
TOPICAL
TE code
AB
Application
ANDA 076973
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of ALCLOMETASONE DIPROPIONATE
- 1982ACLOVATEBrand (NDA)
NDA 018707 · FOUGERA PHARMS
- 1982ACLOVATEBrand (NDA)
NDA 018702 · FOUGERA PHARMS
- 2009ALCLOMETASONE DIPROPIONATEGeneric (ANDA)
ANDA 079227 · GLENMARK PHARMS LTD
- 2009ALCLOMETASONE DIPROPIONATEGeneric (ANDA)
ANDA 079061 · GLENMARK PHARMS LTD
- 2005ALCLOMETASONE DIPROPIONATEGeneric (ANDA)
ANDA 076587 · SUN PHARMA CANADA
- 2005ALCLOMETASONE DIPROPIONATEGeneric (ANDA)
ANDA 076884 · FOUGERA PHARMS
- 2004ALCLOMETASONE DIPROPIONATEGeneric (ANDA)
ANDA 076730 · SUN PHARMA CANADA
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.
