Orange Book product · Generic (ANDA)
SECOBARBITAL SODIUM
SECOBARBITAL SODIUM
At a glance
Approved Prior to Jan 1, 1982
Approved
Generic (ANDA)
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
100MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 084676
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SECOBARBITAL SODIUM
- —SECONAL SODIUMBrand (NDA)
NDA 007392 · LILLY
- 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 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.
