Orange Book product · Generic (ANDA)
ETHOSUXIMIDE
ETHOSUXIMIDE
At a glance
Nov 22, 2000
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 22, 2000
25 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
ETHOSUXIMIDE
Strength
250MG/5ML
Dosage form
SYRUP
Route
ORAL
TE code
AA
Application
ANDA 040253
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ETHOSUXIMIDE
- —ZARONTINBrand (NDA)
NDA 012380 · PARKE DAVIS
- 2020ETHOSUXIMIDEGeneric (ANDA)
ANDA 210654 · PURACAP PHARM LLC
- 2019ETHOSUXIMIDEGeneric (ANDA)
ANDA 211928 · ONESOURCE SPECIALTY
- 2012ETHOSUXIMIDEGeneric (ANDA)
ANDA 200892 · HERITAGE PHARMS INC
- 2008ETHOSUXIMIDEGeneric (ANDA)
ANDA 040686 · EPIC PHARMA LLC
- 2003ETHOSUXIMIDEGeneric (ANDA)
ANDA 040506 · CHARTWELL RX
- 2002ETHOSUXIMIDEGeneric (ANDA)
ANDA 040430 · BIONPHARMA
- 1993ETHOSUXIMIDEGeneric (ANDA)
ANDA 081306 · TEVA PHARMS
- —ZARONTINGeneric (ANDA)
ANDA 080258 · PARKE-DAVIS
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.
