Orange Book product · Generic (ANDA)
FOSPHENYTOIN SODIUM
FOSPHENYTOIN SODIUM
At a glance
Aug 06, 2007
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 06, 2007
19 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
FOSPHENYTOIN SODIUM
Strength
EQ 50MG PHENYTOIN NA/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 078277
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FOSPHENYTOIN SODIUM
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ANDA 078126 · APOTEX INC
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ANDA 078052 · FRESENIUS KABI USA
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ANDA 077481 · HIKMA
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.
