Tacrine therapy
First Claim
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1. An osmotic dosage form for delivering tacrine to the gastrointestinal tract of an Alzheimer'"'"'s patient, wherein the osmotic dosage form comprises:
- (a) a tacrine composition comprising 86.15 mg of tacrine hydrochloride, 86.15 mg of mannitol, 7.25 mg of poly(vinylpyrrolidone) and 1.81 mg of magnesium stearate;
(b) a semipermeable wall coated around the tacrine composition, comprising 80 wt % cellulose acetate and 20 wt % poly(vinylpyrrolidone), and,(c) an exit passageway in the wall that connects the tacrine composition with the exterior of the dosage form for delivering tacrine over 24 hours.
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Abstract
A dosage form is disclosed for administering 10 ng to 1200 mg tacrine to a patient in need of tacrine therapy.
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2 Claims
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1. An osmotic dosage form for delivering tacrine to the gastrointestinal tract of an Alzheimer'"'"'s patient, wherein the osmotic dosage form comprises:
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(a) a tacrine composition comprising 86.15 mg of tacrine hydrochloride, 86.15 mg of mannitol, 7.25 mg of poly(vinylpyrrolidone) and 1.81 mg of magnesium stearate; (b) a semipermeable wall coated around the tacrine composition, comprising 80 wt % cellulose acetate and 20 wt % poly(vinylpyrrolidone), and, (c) an exit passageway in the wall that connects the tacrine composition with the exterior of the dosage form for delivering tacrine over 24 hours. - View Dependent Claims (2)
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Specification