Orange Book product · Generic (ANDA)
DIVALPROEX SODIUM
DIVALPROEX SODIUM
At a glance
Jan 27, 2009
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 27, 2009
17 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
DIVALPROEX SODIUM
Strength
EQ 125MG VALPROIC ACID
Dosage form
CAPSULE, DELAYED REL PELLETS
Route
ORAL
TE code
AB
Application
ANDA 078919
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DIVALPROEX SODIUM
- 2002DEPAKOTE ERBrand (NDA)
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- 1990DEPAKOTE CPBrand (NDA)
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- 1989DEPAKOTEBrand (NDA)
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- 1984DEPAKOTEBrand (NDA)
NDA 018723 · ABBVIE
- 2025DIVALPROEX SODIUMGeneric (ANDA)
ANDA 217358 · MANKIND PHARMA
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ANDA 218793 · ALEMBIC
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ANDA 215527 · ANNORA PHARMA
- 2022DIVALPROEX SODIUMGeneric (ANDA)
ANDA 214643 · UNICHEM
- 2021DIVALPROEX SODIUMGeneric (ANDA)
ANDA 214462 · YICHANG HUMANWELL
- 2020DIVALPROEX SODIUMGeneric (ANDA)
ANDA 211505 · TEVA PHARMS USA
- 2020DIVALPROEX SODIUMGeneric (ANDA)
ANDA 213181 · AJANTA PHARMA LTD
- 2019DIVALPROEX SODIUMGeneric (ANDA)
ANDA 209286 · LUPIN
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.
