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MODIFIED RELEASE 1-[(3-HYDROXY-ADAMANT-1-YLAMINO)-ACETYL]-PYRROLIDINE-2(S)-CARBONITRILE FORMULATION
专利权人:
NOVARTIS AG
发明人:
JAMES KOWALSKI,JAY PARTHIBAN LAKSHMAN,ABU T. M. SERAJUDDIN,YATINDRA JOSHI
申请号:
MYPI 20062526
公开号:
MY152185A
申请日:
2006.06.01
申请国别(地区):
MY
年份:
2014
代理人:
摘要:
THE SUBJECT INVENTION PROVIDES A PHARMACEUTICAL TABLET FORMULATION COMPRISING PER TABLET THE FOLLOWING INGREDIENTS: (A) A COMPOUND AS AN ACTIVE INGREDIENT, WHEREIN THE COMPOUND HAS A FORMULA: WHEREIN R IS SUBSTITUTED ADAMANTYL AND N IS AN INTEGER FROM 0 TO 3 OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF; (B) A HYDROXYPROPYL METHYLCELLULOSE WITH AN APPARENT VISCOSITY OF 80,000 CP TO 120,000 CP (NOMINAL VALUE 100,000 CP) WHEN PRESENT IN A 2% SOLUTION: (C) A MICROCRYSTALLINE CELLULOSE; AND (D) A MAGNESIUM STEARATE THE SUBJECT INVENTION ALSO PROVIDES A PHARMACEUTICAL TABLET FORMULATION, COMPRISING PER 400 MG TABLET THE FOLLOWING INGREDIENTS: (A) 1-[(3—HYDROXY-ADAMANT-1-YLAMINO)—ACETYL]-PYRROLIDINE—2 (S) —CARBONITRILE OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF; (B) A HYDROXYPROPYL METHYLCELLULOSE IN AN AMOUNT OF ABOUT 160 MG, WHEREIN THE HYDROXYPROPYL METHYLCELLULOSE HAS AN APPARENT VISCOSITY OF 80,000 CP TO 120,000 CP (NOMINAL VALUE 100,000 CP) WHEN PRESENT IN A 2% SOLUTION; (C) A MICROCRYSTALLINE CELLULOSE IN AN AMOUNT OF 120 MG; (D) A LACTOSE IN AN AMOUNT OF ABOUT 16 MG; AND (E) A MAGNESIUM STEARATE IN AN AMOUNT OF 4 MG. THE SUBJECT INVENTION ALSO PROVIDES A PHARMACEUTICAL TABLET FORMULATION COMPRISING PER TABLET THE FOLLOWING INGREDIENTS: (C) A COMPOUND AS AN ACTIVE INGREDIENT, WHEREIN THE COMPOUND HAS A FORMULA: WHEREIN R IS SUBSTITUTED ADAMANTYL AND N IS AN INTEGER FROM 0 TO 3; OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF; AND (D) A HYDROXYPROPY) METHYLCELLULOSE WITH AN APPARENT VISCOSITY OF 80,000 CP TO 120,000 CP (NOMINAL VALUE 100,000 CP) WHEN PRESENT IN A 2% SOLUTION.
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中国工程科技知识中心
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