Orange Book product · Generic (ANDA)
CLONIDINE
CLONIDINE
At a glance
Aug 18, 2009
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 18, 2009
17 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
CLONIDINE
Strength
0.1MG/24HR
Dosage form
SYSTEM
Route
TRANSDERMAL
TE code
Not listed
Application
ANDA 076157
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CLONIDINE
- 2009CLONIDINEBrand (NDA)
NDA 022499 · TRIS PHARMA INC
- 2009NEXICLON XRBrand (NDA)
NDA 022500 · ROSEMONT
- 1984CATAPRES-TTS-1Brand (NDA)
NDA 018891 · LAVIPHARM
- 2014CLONIDINEGeneric (ANDA)
ANDA 090873 · ACTAVIS LABS UT INC
- 2010CLONIDINEGeneric (ANDA)
ANDA 079090 · DR REDDYS LABS SA
- 2010CLONIDINEGeneric (ANDA)
ANDA 076166 · MYLAN TECHNOLOGIES
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.
