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PHARMACEUTICAL COMPOSITION CONTAINING IRON OXYHYDROXIDE, METHOD FOR PRODUCING AND APPLICATION
专利权人:
ВИФОР (ИНТЕРНАЦИОНАЛЬ) АГ (CH)
发明人:
ВАЙБЕЛЬ Лудвиг Даниель (CH),ФИЛИПП Эрик (CH)
申请号:
RU2013128356/15
公开号:
RU2013128356A
申请日:
2013.06.20
申请国别(地区):
RU
年份:
2014
代理人:
摘要:
1. A pharmaceutical composition containing iron oxyhydroxide in an amount of from 10 to 80% (by weight) relative to the total weight of the composition, in a form suitable for oral administration, which contains a mixture of native and pregelatinized starch. The pharmaceutical composition according to claim 1, in a form suitable for oral administration in the form of film-coated dosage forms for swallowing in whole form or in the form of dosage forms capable of disintegration in the oral cavity. The composition according to claim 2, which is a dosage form adapted for disintegration in the oral cavity or in a small amount of liquid before swallowing. The composition according to claim 2, in which the dosage form capable of disintegration in the oral cavity is selected from the group consisting of chewable tablets or pills, dry powders, granules, capsules or sachets containing such granules, cachets or lozenges. The composition according to claim 2, the dosage form of which is capable of disintegration in the oral cavity is selected from chewable tablets. The composition according to claim 2, wherein the oral dosage forms are capable of rapid disintegration in the oral cavity or in a small amount of liquid before swallowing, and where iron oxyhydroxide is present in an amount of 700 to 1700 mg per dosage form. The composition according to claim 6, in which iron oxyhydroxide is present in an amount of 800 mg per dosage form. The composition according to claim 1, which contains sucrose. The composition according to claim 1, which consists of iron oxyhydroxide, sucrose, a mixture of native and pregelatinized starch, flavoring, sweetener and a glidant. The composition according to claim 1, in which approx1. Фармацевтическая композиция, содержащая оксигидроксид железа в количестве от 10 до 80% (по весу) относительно общей массы композиции, в форме, подходящей для перорального введения, которая содержит смесь нативного и прежелатинизированного крахмала.2. Фармацевтическая к
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