Orange Book product · Brand (NDA)
SECONAL SODIUM
SECOBARBITAL SODIUM
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
SECOBARBITAL SODIUM
Strength
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 007392
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1983SECONAL SODIUMGeneric (ANDA)
ANDA 086101 · VALEANT PHARMS NORTH
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 084422 · ANABOLIC
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 084225 · BARR
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085895 · EVERYLIFE
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 084676 · HALSEY
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085869 · IVAX PHARMS
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085285 · KV PHARM
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085909 · LANNETT
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085903 · LANNETT
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 084762 · PARKE DAVIS
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 084561 · PERRIGO
- —SECOBARBITAL SODIUMGeneric (ANDA)
ANDA 085867 · PUREPAC PHARM
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.
