STATOL Film-coated tablet Ref.[27882] Active ingredients: Rosuvastatin

Source: Υπουργείο Υγείας (CY)  Revision Year: 2021  Publisher: Delorbis Pharmaceuticals Ltd., 17 Athinon Street, Ergates Industrial Area, 2643 Ergates, P.O. Box 28629, 2081 Lefkosia, Cyprus, European Union

Product name and form

Statol 5 mg film-coated tablets.

Statol 10 mg film-coated tablets.

Statol 20 mg film-coated tablets.

Statol 40 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablets.

5 mg: Yellow, round, biconvex, coated tablet, embossed ‘ROS’ over ‘5’ on one side and nothing on the other, with diameter 7 mm.

10 mg: Pink, round, biconvex, coated tablet, embossed ‘ROS’ over ‘10’ on one side and nothing on the other, with diameter 7 mm.

20 mg: Pink, round, biconvex, coated tablet, embossed ‘ROS’ over ‘20’ on one side and nothing on the other, with diameter 9 mm.

40 mg: Pink, oval, biconvex, coated tablet, embossed ‘ROS’ on one side and ‘40’ on the other side, with dimensions 6.8 × 11.4 mm.

Qualitative and quantitative composition

5 mg

Each tablet contains 5 mg rosuvastatin (as rosuvastatin calcium).

Excipient(s) with known effect:

Each tablet contains 100.915 mg lactose monohydrate.

10 mg

Each tablet contains 10 mg rosuvastatin (as rosuvastatin calcium).

Excipient(s) with known effect:

Each tablet contains 95.706 mg lactose monohydrate.

20 mg

Each tablet contains 20 mg rosuvastatin (as rosuvastatin calcium).

Excipient(s) with known effect:

Each tablet contains 191.412 mg lactose monohydrate.

40 mg

Each tablet contains 40 mg rosuvastatin (as rosuvastatin calcium).

Excipient(s) with known effect:

Each tablet contains 172.824 mg lactose monohydrate.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Rosuvastatin

Rosuvastatin is a selective and competitive inhibitor of HMG-CoA reductase. Rosuvastatin increases the number of hepatic LDL receptors on the cell-surface, enhancing uptake and catabolism of LDL and it inhibits the hepatic synthesis of VLDL, thereby reducing the total number of VLDL and LDL particles.

List of Excipients

Tablet core:

Microcrystalline cellulose
Colloidal anhydrous silica
Crospovidone Type A
Lactose monohydrate
Magnesium stearate

Tablet coat:

5 mg tablet: Opadry II Yellow 33K12488 (Hypromellose, titanium dioxide (E171), lactose monohydrate, triacetin, iron oxide yellow (E172)).

10 mg tablet: Opadry II Pink 33K94423 (Hypromellose, titanium dioxide (E171), lactose monohydrate, triacetin, iron oxide red (E172)).

20 mg tablet: Opadry II Pink 33K94423 (Hypromellose, titanium dioxide (E171), lactose monohydrate, triacetin, iron oxide red (E172)).

40 mg tablet: Opadry II Pink 33K94424 (Hypromellose, titanium dioxide (E171), lactose monohydrate, triacetin, iron oxide red (E172)).

Pack sizes and marketing

OPA-Al-PVC/Al blisters.

Pack sizes: 14, 20, 28, 30, 56, 60, 84, 90 and 100 film-coated tablets.

Not all pack sizes may be marketed.

Marketing authorization holder

Delorbis Pharmaceuticals Ltd., 17 Athinon Street, Ergates Industrial Area, 2643 Ergates, P.O. Box 28629, 2081 Lefkosia, Cyprus, European Union

Marketing authorization dates and numbers

Statol 5 mg film-coated tablets: 022934
Statol 10 mg film-coated tablets: 022935
Statol 20 mg film-coated tablets: 022936
Statol 40 mg film-coated tablets: 022937

Date of first authorisation: 22/04/2019

Drugs

Drug Countries
STATOL Cyprus, Malta

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