Orange Book product · Generic (ANDA)
THIOTHIXENE
THIOTHIXENE
At a glance
Jun 23, 1987
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 23, 1987
39 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
THIOTHIXENE
Strength
1MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 071093
Product number
002
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of THIOTHIXENE
- —NAVANEBrand (NDA)
NDA 016584 · PFIZER
- 2022THIOTHIXENEGeneric (ANDA)
ANDA 215456 · AMNEAL
- 2019THIOTHIXENEGeneric (ANDA)
ANDA 211642 · NOVITIUM PHARMA
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 072200 · AM THERAP
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071884 · AM THERAP
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071885 · AM THERAP
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071886 · AM THERAP
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071887 · AM THERAP
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071626 · WATSON LABS
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071627 · WATSON LABS
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071628 · WATSON LABS
- 1987THIOTHIXENEGeneric (ANDA)
ANDA 071529 · EPIC PHARMA LLC
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.
