Orange Book product · Generic (ANDA)
CHLOROTHIAZIDE
CHLOROTHIAZIDE
At a glance
Sep 01, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 01, 1982
44 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLOROTHIAZIDE
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 084026
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CHLOROTHIAZIDE
- —DIURILBrand (NDA)
NDA 011870 · SALIX PHARMS
- —DIURILBrand (NDA)
NDA 011145 · RISING
- 1983CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086795 · WATSON LABS
- 1983CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086796 · WATSON LABS
- 1982CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086028 · HIKMA INTL PHARMS
- 1982CHLOROTHIAZIDEGeneric (ANDA)
ANDA 087736 · HIKMA INTL PHARMS
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 085569 · ABC HOLDING
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086940 · LEDERLE
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086938 · LEDERLE
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 084217 · PHARMOBEDIENT
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 085485 · SANDOZ
- —CHLOROTHIAZIDEGeneric (ANDA)
ANDA 085165 · WATSON LABS
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.
