Orange Book product · Generic (ANDA)
BUTABARBITAL SODIUM
BUTABARBITAL SODIUM
At a glance
May 18, 1985
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 18, 1985
41 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
BUTABARBITAL SODIUM
Strength
15MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 088632
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of BUTABARBITAL SODIUM
- —BUTISOL SODIUMBrand (NDA)
NDA 000793 · PHARMOBEDIENT
- 1985BUTABARBITAL SODIUMGeneric (ANDA)
ANDA 088631 · TEVA
- 1982BUTABARBITAL SODIUMGeneric (ANDA)
ANDA 084292 · SANDOZ
- —BUTICAPSGeneric (ANDA)
ANDA 085381 · MEDPOINTE PHARM HLC
- —BUTABARBGeneric (ANDA)
ANDA 085873 · ALPHARMA US PHARMS
- —BUTABARBITAL SODIUMGeneric (ANDA)
ANDA 085383 · WOCKHARDT
- —BUTALANGeneric (ANDA)
ANDA 085880 · LANNETT
- —BUTISOL SODIUMGeneric (ANDA)
ANDA 085380 · MEDA PHARMS
- —SARISOLGeneric (ANDA)
ANDA 084723 · HALSEY
- —BUTABARBITALGeneric (ANDA)
ANDA 085550 · BUNDY
- —BUTABARBITAL SODIUMGeneric (ANDA)
ANDA 085938 · SANDOZ
- —BUTABARBITAL SODIUMGeneric (ANDA)
ANDA 084272 · SANDOZ
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.
