US2007254031A1PendingUtilityA1
Rapidly disintegrable solid preparation
Est. expiryJul 28, 2018(expired)· nominal 20-yr term from priority
A61P 7/00A61P 5/00A61P 9/12A61P 43/00A61P 9/00A61P 3/10A61P 3/00A61P 15/00A61P 13/00A61P 1/00A61P 11/00A61P 1/04A61K 9/0056A61K 31/41A61K 9/2054A61K 31/13A61K 9/2018A61K 31/717A61K 9/2081A61K 9/20
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Claims
Abstract
A rapidly disintegrable solid preparation which comprises (i) a pharmacologically active ingredient, (ii) a sugar and (iii) a low-substituted hydroxypropylcellulose having 5 % by weight or more to less than 7 % by weight of hydroxypropoxyl group. The rapidly disintegrable solid preparation has fast disintegrability, suitable strength and no roughness.
Claims
exact text as granted — not AI-modified1 . An orally rapidly disintegrable solid preparation which comprises (i) a pharmacologically active ingredient, (ii) a sugar and (iii) a low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl group, wherein said solid preparation is bucally dissolved in from about 5 to about 50 seconds.
2 . (canceled)
3 . A preparation of claim 1 , which is a tablet.
4 . A preparation of claim 1 , wherein the sugar is a sugar alcohol.
5 . A preparation of claim 4 , wherein the sugar alcohol is mannitol or erythritol.
6 . A preparation of claim 1 , wherein the sugar is in an amount of 5 to 97 parts by weight per 100 parts by weight of the solid preparation.
7 . A preparation of claim 1 , wherein the low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl group is used in an amount of 3 to 50 parts by weight per 100 parts by weight of the solid preparation.
8 . (canceled)
9 . A preparation of claim 1 , wherein the pharmacologically active ingredient is voglibose.
10 . (canceled)
11 . (canceled)
12 . A preparation of claim 1 , wherein the pharmacologically active ingredient is candesartan cilexetil.
13 . A preparation of claim 3 which comprises fine granules.
14 . A preparation of claim 13 , wherein the pharmacologically active ingredient is comprised in fine granules of the solid preparation.
15 . A preparation of claim 14 , wherein (i) a sugar and (ii) a low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl group are comprised in the solid preparation separately from fine granules.
16 . A preparation of claim 15 , wherein the sugar is in an amount of 5 to 97 parts by weight per 100 parts by weight of the rest of the solid preparation other than the fine granules.
17 . A preparation of the claim 15 , wherein the low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl group is in an amount of 3 to 50 parts by weight per 100 parts by weight of the rest of the solid preparation other than the fine granules.
18 . (canceled)
19 . (canceled)Join the waitlist — get patent alerts
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