Orange Book product · Generic (ANDA)
HALOBETASOL PROPIONATE
HALOBETASOL PROPIONATE
At a glance
Dec 16, 2004
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 16, 2004
21 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
HALOBETASOL PROPIONATE
Strength
0.05%
Dosage form
CREAM
Route
TOPICAL
TE code
AB
Application
ANDA 077123
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HALOBETASOL PROPIONATE
- 2018BRYHALIBrand (NDA)
NDA 209355 · BAUSCH
- 2018LEXETTEBrand (NDA)
NDA 210566 · MAYNE PHARMA
- 2015ULTRAVATEBrand (NDA)
NDA 208183 · LACER PHARMA
- 1990ULTRAVATEBrand (NDA)
NDA 019967 · SUN PHARM INDS INC
- 1990ULTRAVATEBrand (NDA)
NDA 019968 · SUN PHARM INDS INC
- 2023HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 215266 · PADAGIS ISRAEL
- 2020HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 213560 · QUAGEN
- 2020HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 211464 · PADAGIS ISRAEL
- 2018HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 209978 · ENCUBE
- 2007HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 078162 · COSETTE PHARMS NC
- 2006HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 077721 · COSETTE
- 2005HALOBETASOL PROPIONATEGeneric (ANDA)
ANDA 077227 · 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.
