Orange Book product · Generic (ANDA)
PREDNISOLONE SODIUM PHOSPHATE
PREDNISOLONE SODIUM PHOSPHATE
At a glance
Apr 10, 2013
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 10, 2013
13 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
PREDNISOLONE SODIUM PHOSPHATE
Strength
EQ 10MG BASE
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
TE code
Not listed
Application
ANDA 202179
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
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ANDA 216715 · AMNEAL
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ANDA 204962 · PHARM ASSOC
- 2016PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 203559 · EDENBRIDGE PHARMS
- 2010PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 091396 · MISSION PHARMA
- 2009PREDNISOLONE SODIUM PHOSPHATEGeneric (ANDA)
ANDA 079010 · PH HEALTH
- 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.
