Orange Book product · Generic (ANDA)
PREDNISOLONE
PREDNISOLONE
At a glance
Sep 21, 2007
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 21, 2007
19 yr ago
Today
Pharmaceutical detail
Active ingredient
PREDNISOLONE
Strength
15MG/5ML
Dosage form
SOLUTION
Route
ORAL
TE code
AA
Application
ANDA 040775
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PREDNISOLONE
- —METI-DERMBrand (NDA)
NDA 010209 · SCHERING
- —DELTA-CORTEFBrand (NDA)
NDA 009987 · PHARMACIA AND UPJOHN
- 2025PREDNISOLONEGeneric (ANDA)
ANDA 219509 · TP ANDA HOLDINGS
- 2023PREDNISOLONEGeneric (ANDA)
ANDA 215673 · AUROBINDO PHARMA LTD
- 2005PREDNISOLONEGeneric (ANDA)
ANDA 040571 · PHARM ASSOC
- 2005PREDNISOLONEGeneric (ANDA)
ANDA 040570 · PHARM ASSOC
- 2003PREDNISOLONEGeneric (ANDA)
ANDA 040313 · PHARMOBEDIENT CNSLTG
- 2003PREDNISOLONEGeneric (ANDA)
ANDA 040399 · PHARM ASSOC
- 2003PREDNISOLONEGeneric (ANDA)
ANDA 040401 · HIKMA
- 2002PREDNISOLONEGeneric (ANDA)
ANDA 040364 · NESHER PHARMS
- 2001PREDNISOLONEGeneric (ANDA)
ANDA 040423 · NESHER PHARMS
- 2000PREDNISOLONEGeneric (ANDA)
ANDA 040322 · TEVA PHARMS
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.
