Orange Book product · Generic (ANDA)
CHLORTHALIDONE
CHLORTHALIDONE
At a glance
Jul 21, 1986
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 21, 1986
40 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLORTHALIDONE
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 089286
Product number
002
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CHLORTHALIDONE
- 2024CHLORTHALIDONEGeneric (ANDA)
ANDA 209162 · IPCA LABS LTD
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 216262 · ALEMBIC
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 215587 · MANKIND PHARMA
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 212878 · PHARMOBEDIENT
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 212875 · PHARMOBEDIENT
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 211320 · INVENTIA
- 2022CHLORTHALIDONEGeneric (ANDA)
ANDA 209068 · SUNNY
- 2020CHLORTHALIDONEGeneric (ANDA)
ANDA 214129 · AJANTA PHARMA LTD
- 2020CHLORTHALIDONEGeneric (ANDA)
ANDA 213412 · ALKEM LABS LTD
- 2019CHLORTHALIDONEGeneric (ANDA)
ANDA 211627 · UNICHEM
- 2019CHLORTHALIDONEGeneric (ANDA)
ANDA 207204 · AMNEAL PHARMS CO
- 2019CHLORTHALIDONEGeneric (ANDA)
ANDA 211063 · CHARTWELL RX
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.

