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Treats Attention Deficit Hyperactivity Disorder (ADHD). Sold as Catapres, Duraclon, Jenloga, Kapvay, Onyda Xr and 2 more. Every FDA application for this active ingredient: 6 branded and 54 generic.
As of Nov 15, 2026, FDA lists 60 applications for Clonidine Hydrochloride (sold as Catapres, Duraclon, Jenloga and others), first approved Sep 3, 1974, with 4 new uses approved and 0 published complete response letters.
First approved: Sep 3, 1974
Applications: 60
New uses approved: 4
Complete response letters: 0
Medicare spending, 2025: $24.3M
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
Clonidine HCl
Part D
$22.3M
-1%
907,402
Clonidine HCl ER
Part D
$1.9M
+40%
4,645
Onyda XR
Part D
$95K
New
41
Javadin
Part D
$0K
New
0
What Pharmacies Pay
Median price per unit across package codes in CMS's weekly NADAC survey, Nov 11, 2026, before rebates; see every drug's price change
CLONIDINE 0.1 MG/DAY PATCH: $6.54 per unitGeneric · -5% in a year
CLONIDINE 0.2 MG/DAY PATCH: $8.77 per unitGeneric · -7% in a year
CLONIDINE 0.3 MG/DAY PATCH: $12.38 per unitGeneric · +6% in a year
CLONIDINE HCL 0.05 MG TABLET: $1.17 per unitGeneric · new this year
CLONIDINE HCL 0.1 MG TABLET: $0.023 per unitGeneric · -6% in a year
CLONIDINE HCL 0.2 MG TABLET: $0.034 per unitGeneric · -4% in a year
CLONIDINE HCL 0.3 MG TABLET: $0.041 per unitGeneric · 0% in a year
CLONIDINE HCL ER 0.1 MG TABLET: $0.224 per unitGeneric · -20% in a year
CLONIDINE HCL ER 0.17 MG TAB: $15.21 per unitGeneric · +4% in a year
ONYDA XR 0.1 MG/ML SUSPENSION: $13.37 per MLBrand · +31% in a year
JAVADIN 0.02 MG/ML SOLUTION: $1.53 per MLBrand · new this year
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA