Orange Book product · Generic (ANDA)
CLONIDINE HYDROCHLORIDE
CLONIDINE HYDROCHLORIDE
At a glance
Apr 06, 2026
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 06, 2026
2 mo ago
Today
Pharmaceutical detail
Active ingredient
CLONIDINE HYDROCHLORIDE
Strength
0.05MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 070923
Product number
004
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CLONIDINE HYDROCHLORIDE
- 2025JAVADINBrand (NDA)
NDA 220256 · AZURITY
- 2024ONYDA XRBrand (NDA)
NDA 217645 · TRIS PHARMA INC
- 2009JENLOGABrand (NDA)
NDA 022331 · CONCORDIA PHARMS INC
- 1996DURACLONBrand (NDA)
NDA 020615 · MYLAN INSTITUTIONAL
- —CATAPRESBrand (NDA)
NDA 017407 · BOEHRINGER INGELHEIM
- 2019CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209675 · NOVAST LABS
- 2018CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 211433 · SOMERSET THERAPS LLC
- 2018CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 210680 · RUBICON RESEARCH
- 2018CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 210338 · JUBILANT GENERICS
- 2017CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209686 · AJANTA PHARMA LTD
- 2017CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 210052 · AMNEAL PHARMS NY
- 2017CLONIDINE HYDROCHLORIDEGeneric (ANDA)
ANDA 209757 · XIAMEN LP PHARM CO
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.
