Orange Book product · Generic (ANDA)
HYDROCORTISONE BUTYRATE
HYDROCORTISONE BUTYRATE
At a glance
Jan 14, 2004
Approved
Generic (ANDA)
Application
AT
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 14, 2004
22 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCORTISONE BUTYRATE
Strength
0.1%
Dosage form
SOLUTION
Route
TOPICAL
TE code
AT
Application
ANDA 076364
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCORTISONE BUTYRATE
- 2007LOCOIDBrand (NDA)
NDA 022076 · BAUSCH
- 1997LOCOID LIPOCREAMBrand (NDA)
NDA 020769 · PRECISION DERMAT
- 1988LOCOIDBrand (NDA)
NDA 019819 · YAMANOUCHI
- 1987LOCOIDBrand (NDA)
NDA 019116 · BAUSCH
- 1984LOCOIDBrand (NDA)
NDA 019106 · YAMANOUCHI
- 1983LOCOIDBrand (NDA)
NDA 018795 · YAMANOUCHI
- 1982LOCOIDBrand (NDA)
NDA 018652 · PRECISION DERMAT
- 1982LOCOIDBrand (NDA)
NDA 018514 · BAUSCH
- 2018HYDROCORTISONE BUTYRATEGeneric (ANDA)
ANDA 210209 · LUPIN
- 2017HYDROCORTISONE BUTYRATEGeneric (ANDA)
ANDA 205134 · ACTAVIS MID ATLANTIC
- 2017HYDROCORTISONE BUTYRATEGeneric (ANDA)
ANDA 209556 · THE J MOLNER
- 2013HYDROCORTISONE BUTYRATEGeneric (ANDA)
ANDA 202145 · GLENMARK PHARMS LTD
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.
