Orange Book product · Generic (ANDA)
CHLOROTHIAZIDE SODIUM
CHLOROTHIAZIDE SODIUM
At a glance
May 29, 2015
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 29, 2015
11 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLOROTHIAZIDE SODIUM
Strength
EQ 500MG BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 202462
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CHLOROTHIAZIDE SODIUM
- —DIURILBrand (NDA)
NDA 011145 · RISING
- 2024CHLOROTHIAZIDE SODIUMGeneric (ANDA)
ANDA 218630 · GLAND
- 2014CHLOROTHIAZIDE SODIUMGeneric (ANDA)
ANDA 202493 · RK PHARMA
- 2013CHLOROTHIAZIDE SODIUMGeneric (ANDA)
ANDA 202561 · AM REGENT
- 2011CHLOROTHIAZIDE SODIUMGeneric (ANDA)
ANDA 091546 · SUN PHARM
- 2009CHLOROTHIAZIDE SODIUMGeneric (ANDA)
ANDA 090896 · FRESENIUS KABI USA
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.
