Rapidly disintegrable solid preparation
AssigneeTakeda Pharmaceutical Company Limited
InventorsToshihiro Shimizu, Masae Sugaya, Yoshinori Nakano
Life of this patent
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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.
Claims2
An oral rapidly disintegrable solid preparation which comprises (i) manidipine hydrochloride, (ii) a sugar and (iii) a low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl groups;
- wherein said solid preparation is buccally dissolved in from about 5 to about 50 seconds.
An oral rapidly disintegrable solid preparation which comprises (i) pioglitazone hydrochloride, (ii) a sugar and (iii) a low-substituted hydroxypropylcellulose having 5% by weight or more to less than 7% by weight of hydroxypropoxyl groups;
- wherein said solid preparation is buccally dissolved in from about 5 to about 50 seconds.
Dependencies are inferred from the claim text.