Orange Book product · Brand (NDA)
DIURIL
CHLOROTHIAZIDE
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
CHLOROTHIAZIDE
Strength
250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 011145
Product number
004
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- —DIURILBrand (NDA)
NDA 011870 · SALIX PHARMS
- 1983CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086795 · WATSON LABS
- 1983CHLOROTHIAZIDEGeneric (ANDA)
ANDA 086796 · WATSON LABS
- 1982CHLOROTHIAZIDEGeneric (ANDA)
ANDA 084026 · 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.
