Orange Book product · Brand (NDA)
TOLBUTAMIDE
TOLBUTAMIDE
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
TOLBUTAMIDE
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 012678
Product number
001
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.
- —ORINASEBrand (NDA)
NDA 010670 · PHARMACIA AND UPJOHN
- 1987TOLBUTAMIDEGeneric (ANDA)
ANDA 089110 · WATSON LABS
- 1987TOLBUTAMIDEGeneric (ANDA)
ANDA 089111 · WATSON LABS
- 1985TOLBUTAMIDEGeneric (ANDA)
ANDA 088950 · PUREPAC PHARM
- 1984TOLBUTAMIDEGeneric (ANDA)
ANDA 088893 · SUPERPHARM
- 1983TOLBUTAMIDEGeneric (ANDA)
ANDA 087541 · ASCOT
- 1982TOLBUTAMIDEGeneric (ANDA)
ANDA 087876 · VANGARD
- —TOLBUTAMIDEGeneric (ANDA)
ANDA 086141 · ALRA
- —TOLBUTAMIDEGeneric (ANDA)
ANDA 087093 · ANI PHARMS
- —TOLBUTAMIDEGeneric (ANDA)
ANDA 087121 · BARR
- —TOLBUTAMIDEGeneric (ANDA)
ANDA 086574 · CHARTWELL RX
- —TOLBUTAMIDEGeneric (ANDA)
ANDA 086926 · DAVA PHARMS INC
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.
