Orange Book product · Generic (ANDA)
PREDNISOLONE SODIUM PHOSPHATE
PREDNISOLONE SODIUM PHOSPHATE
At a glance
May 26, 2009
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 26, 2009
17 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
PREDNISOLONE SODIUM PHOSPHATE
Strength
EQ 15MG BASE/5ML
Dosage form
SOLUTION
Route
ORAL
TE code
Not listed
Application
ANDA 079010
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PREDNISOLONE SODIUM PHOSPHATE
- 2006ORAPRED ODTBrand (NDA)
NDA 021959 · ADVANZ PHARMA
- 1986PEDIAPREDBrand (NDA)
NDA 019157 · PAI HOLDINGS
- —HYDELTRASOLBrand (NDA)
NDA 011583 · MERCK
- —HYDELTRASOLBrand (NDA)
NDA 011028 · MERCK
- 2022PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 216715 · AMNEAL
- 2020PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 204962 · PHARM ASSOC
- 2016PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 203559 · EDENBRIDGE PHARMS
- 2013PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 202179 · RISING
- 2010PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 091396 · MISSION PHARMA
- 2009PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 078345 · AMNEAL PHARMS
- 2008PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 078988 · PHARM ASSOC
- 2008PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 078465 · PHARM ASSOC
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.
