FIELD: chemical-pharmaceutical industry, pharmacy.
SUBSTANCE: invention relates to a solid standard dosed formulation comprising atorvastatin or its pharmaceutically acceptable salt and a vehicle, or combination of vehicles that comprises above 50 wt.-% of diluting agents and less 5 wt.-% of alkaline substance as an additive. Indicated diluting agent represents lactose monohydrate, anhydrous lactose, microcrystalline cellulose or sodium chloride. The solid standard dosed formulation represents a table or capsule that is made without granulation step. Invention provides preventing segregation during making the standard dosed formulation and to provides the high dosing precision of atorvastatin. Excluding the granulation step results to enhancing effectiveness in producing the standard dosed medicinal formulation and without decreasing the rate of production of composition.
EFFECT: improved and valuable properties of compositions.
5 cl, 1 dwg, 3 tbl, 7 ex
Title | Year | Author | Number |
---|---|---|---|
PHARMACEUTICAL FORMULATION OF ATORVASTATIN | 2004 |
|
RU2325903C2 |
STABLE ATORVASTATIN COMPOSITIONS OBTAINED BY HUMID GRANULATION | 2004 |
|
RU2332211C2 |
PHARMACEUTICAL COMPOSITIONS COMPRISING 5,8,14-TRIAZATETRACYCLO[10,3,1,0(2,11),0(4,9)HEXADECA-2( 11),3,5,7,9-PENTAENE | 2002 |
|
RU2272629C2 |
ORAL ANTITUMOUR DRUGS AND METHOD FOR ONCOLOGICAL DISEASES TREATMENT | 2016 |
|
RU2639479C1 |
METHOD OF TREATMENT OF PATIENTS WITH BACTERIAL INFECTION | 1995 |
|
RU2128998C1 |
TOFACITINIB ORAL SUSTAINED RELEASE DOSAGE FORMS | 2014 |
|
RU2674345C2 |
PHARMACEUTICAL MEDICAL FORM OF ATORVASTATIN | 2005 |
|
RU2395280C2 |
ORAL DOSAGE FORMS OF TOFACITINIB WITH CONTINUOUS RELEASE | 2014 |
|
RU2790166C2 |
METHOD OF OBTAINING COMPOSITIONS BY EXTRUSION OF RESISTANT TO PRESSING PHARMACEUTICAL SUBSTANCES | 2006 |
|
RU2405539C2 |
TAMZULOSIN TABLETS | 2002 |
|
RU2311903C2 |
Authors
Dates
2008-01-20—Published
2004-06-01—Filed