Orange Book product · Generic (ANDA)
VALPROATE SODIUM
VALPROATE SODIUM
Generic (ANDA)ANDA 076539TE APRX FRESENIUS KABI USA
At a glance
Jun 26, 2003
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 26, 2003
23 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
VALPROATE SODIUM
Strength
EQ 100MG BASE/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 076539
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of VALPROATE SODIUM
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.
