Orange Book product · Generic (ANDA)
THIORIDAZINE HYDROCHLORIDE
THIORIDAZINE HYDROCHLORIDE
At a glance
Aug 16, 1996
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 16, 1996
30 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
THIORIDAZINE HYDROCHLORIDE
Strength
30MG/ML
Dosage form
CONCENTRATE
Route
ORAL
TE code
Not listed
Application
ANDA 040125
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of THIORIDAZINE HYDROCHLORIDE
- —MELLARILBrand (NDA)
NDA 011808 · NOVARTIS
- 1998THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040213 · PHARM ASSOC
- 1997THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040187 · PHARM ASSOC
- 1996THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 040126 · EPIC PHARMA LLC
- 1988THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089764 · PAR PHARM
- 1988THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089765 · PAR PHARM
- 1987THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089602 · ANI PHARMS
- 1987THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 089603 · ANI PHARMS
- 1986THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 088136 · CHARTWELL RX
- 1986THIORIDAZINE HYDROCHLORIDEGeneric (ANDA)
ANDA 088137 · CHARTWELL RX
- 1985THIORIDAZINE HYDROCHLORIDE INTENSOLGeneric (ANDA)
ANDA 088941 · ROXANE
- 1985THIORIDAZINE HYDROCHLORIDE INTENSOLGeneric (ANDA)
ANDA 088942 · ROXANE
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.
