Orange Book product · Generic (ANDA)
HYDROCORTISONE ACETATE
HYDROCORTISONE ACETATE
At a glance
Jan 03, 1989
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 03, 1989
38 yr ago
Today
Pharmaceutical detail
Active ingredient
HYDROCORTISONE ACETATE
Strength
1%
Dosage form
CREAM
Route
TOPICAL
TE code
Not listed
Application
ANDA 089914
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCORTISONE ACETATE
- 1982CORTIFOAMBrand (NDA)
NDA 017351 · VIATRIS
- —CORTEF ACETATEBrand (NDA)
NDA 009378 · PHARMACIA AND UPJOHN
- —CORTRILBrand (NDA)
NDA 009164 · PFIZER
- —HYDROCORTISONE ACETATEBrand (NDA)
NDA 009637 · EPIC PHARMA LLC
- —HYDROCORTONEBrand (NDA)
NDA 008228 · MERCK
- —HYDROCORTONEBrand (NDA)
NDA 009018 · MERCK
- —CORTEF ACETATEBrand (NDA)
NDA 008917 · PHARMACIA AND UPJOHN
- 2002MICORT-HCGeneric (ANDA)
ANDA 040398 · LEGACY PHARMA
- 2001MICORT-HCGeneric (ANDA)
ANDA 040396 · LEGACY PHARMA
- 1999HYDROCORTISONE ACETATEGeneric (ANDA)
ANDA 040259 · IMPERIUM
- 1992HEMSOL-HCGeneric (ANDA)
ANDA 081274 · ABLE
- 1988U-CORTGeneric (ANDA)
ANDA 089472 · 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.
