US Patent

US8916588 — Methods for treatment of attention deficit hyperactivity disorder

Method of Use · Assigned to Ironshore Pharmaceuticals and Development Inc Cayman Island · Expires 2032-03-23 · 6y remaining

Vulnerability score 68/100 Moderate — design-around opportunities exist

What this patent protects

This patent protects methods for treating attention deficit disorder or attention deficit hyperactivity disorder using delayed and controlled release formulations of active drug.

USPTO Abstract

Therapeutic compositions and methods for treatment of attention deficit disorder (ADD) or attention deficit hyperactivity disorder (ADHD) include dosage forms that deliver a therapeutic amount of active drug in a delayed and controlled release formulation. The dosage form can be administered at night and drug release is delayed for from 4 to 6 hours or longer, followed by an ascending release rate.

Drugs covered by this patent

FDA Patent Use Codes

When a patent is method-of-use, FDA lists it once per applicable indication ("U-code"). Each U-code carves out a specific therapeutic use that generic filers must either license or design around.

CodeDescriptionDrug
U-2357 methylphenidate-hydrochloride
U-2357 methylphenidate-hydrochloride
U-2357 methylphenidate-hydrochloride
U-2357 methylphenidate-hydrochloride
U-2357 methylphenidate-hydrochloride

Patent Metadata

Patent number
US8916588
Jurisdiction
US
Classification
Method of Use
Expires
2032-03-23
Drug substance claim
No
Drug product claim
No
Assignee
Ironshore Pharmaceuticals and Development Inc Cayman Island
Source
FDA Orange Book + USPTO grounding via Google Patents

Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.

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