
UB510
ProductClonidine Hydrochloride Sustained-Release Tablet
Strength0.1mg
IndicationsAttention deficit/hyperactivity disorder
TherapeuticsPsychiatry
GMPUS - FDA
RegistrationUnited States; China
ModalitiesSmall Molecule
Exclusive Summary
- - Core compound is long off-patent; ER formulation patents have expired in major markets, with multiple US generics, indicating low global IP barriers.
- - ADHD affects ~5–7% of children worldwide (≈60–90 million), creating steady demand for non-stimulants where ER clonidine fits as second-line/adjunct.
- - ER clonidine availability is limited outside the US, offering first/early generic entry opportunities in markets currently dominated by IR clonidine.
- - US-FDA GMP and US registration provide strong compliance credentials for reliance/abridged pathways and fast distribution rollout.
- - Compared with brands and other non-stimulants (e.g., guanfacine ER, atomoxetine), generic ER clonidine can deliver substantial per-day cost reductions (often 70–90% vs. brand).
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