US2021308044A1PendingUtilityA1
Pharmaceutical suspension for oral dosage
Est. expiryAug 18, 2038(~12.1 yrs left)· nominal 20-yr term from priority
A61K 31/513A61K 47/14A61K 31/519A61K 31/423A61K 47/38A61K 9/10A61K 45/06A61K 47/06A61K 31/137A61K 31/554A61K 9/0053A61K 31/5377A61K 47/10A61K 47/26A61K 31/4985A61K 47/02A61K 47/34A61K 47/12
75
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Claims
Abstract
Disclosed herein are pharmaceutical compositions in the form of a suspension for oral delivery. Some embodiments provide a pharmaceutical composition in the form of a suspension for oral delivery comprising an active pharmaceutical ingredient; water; a suspending agent; a buffering agent; and one or more of a wetting agent and a binder/filler. In some embodiments, the active pharmaceutical ingredient is selected from quetiapine, sildenafil, tadalafil, cinacalcet, ticagrelor, mycophenolate, aprepitant, zonisamide, and primidone.
Claims
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22 . A pharmaceutical composition in the form of a suspension for oral delivery comprising:
(a) aprepitant; (b) water; (c) 2 mg/mL to about 3.5 mg/mL xanthan gum as a suspending agent; (d) a buffering agent in an amount sufficient to make the composition pH about 3.5 to about 7; (e) wetting agent consisting of a combination of glycerin and poloxamer; and (f) a binder/filler.
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24 . The pharmaceutical composition of claim 22 , wherein the wetting agent comprises 100 mg/mL glycerin.
25 . The pharmaceutical composition of claim 22 , wherein the binder/filler is selected from one or more binders or fillers selected from acacia, agar, alginic acid, carmellose sodium, dextrin, veegum or gel white, gellan gum, sodium alginate, hydroxypropyl starch, maltodextrin, modified starch, pectin, potassium alginate, polyvinyl pyrrolidone, carboxymethyl cellulose or an alkali metal salt thereof, microcrystalline cellulose, bentonite, colloidal silicon dioxide, microcrystalline cellulose/sodium carboxymethylcellulose, and any combination thereof.
26 . The pharmaceutical composition of claim 22 wherein the binder/filler is microcrystalline cellulose/sodium carboxymethylcellulose.
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30 . The pharmaceutical composition of claim 22 , wherein the buffering agent is selected from group consisting of citrate, citric acid monohydrate or disodium hydrogen phosphate.
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