Orange Book product · Generic (ANDA)
HYDROCORTISONE VALERATE
HYDROCORTISONE VALERATE
At a glance
Aug 12, 1998
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 12, 1998
28 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCORTISONE VALERATE
Strength
0.2%
Dosage form
CREAM
Route
TOPICAL
TE code
Not listed
Application
ANDA 074489
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCORTISONE VALERATE
- 1983WESTCORTBrand (NDA)
NDA 018726 · SUN PHARM INDS INC
- —WESTCORTBrand (NDA)
NDA 017950 · SUN PHARM INDS INC
- 2021HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 211047 · ENCUBE ETHICALS
- 2021HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 213724 · COSETTE PHARMS NC
- 2020HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 211764 · COSETTE PHARMS NC
- 2019HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 210307 · LUPIN
- 2018HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 211750 · GLENMARK PHARMS LTD
- 2018HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 211129 · GLENMARK PHARMS LTD
- 2001HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 075085 · FOUGERA PHARMS
- 2000HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 075666 · PADAGIS ISRAEL
- 1998HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 075042 · SUN PHARMA CANADA
- 1998HYDROCORTISONE VALERATEGeneric (ANDA)
ANDA 075043 · 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.
