Orange Book product · Brand (NDA)
CLONIDINE
CLONIDINE
At a glance
Dec 03, 2009
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 03, 2009
16 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
CLONIDINE
Strength
EQ 0.09MG BASE/ML
Dosage form
SUSPENSION, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 022499
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 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
- 2009CLONIDINEGeneric (ANDA)
ANDA 076157 · DIFGEN PHARMS
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.
