Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2018 Publisher: Generics [UK] Ltd t/a Mylan, Station Close, Potters Bar, Herts, EN6 1TL
Bezafibrate 200 mg Film-coated Tablets.
Pharmaceutical Form |
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Film-coated tablet. Bezafibrate 200 mg Film-coated Tablets are 10mm, round normal convex white film-coated tablets, debossed “BZ/200” on one side and “G” on the other. |
Each tablet contains: 200 mg of bezafibrate.
Excipient with known effect: Each tablet contains 1.56 mg lactose.
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Bezafibrate |
Bezafibrate lowers elevated blood lipids (triglycerides and cholesterol). Elevated VLDL and LDL are reduced by treatment with bezafibrate, whilst HDL-levels are increased. Furthermore, cholesterol biosynthesis is reduced by bezafibrate, which is accompanied by a stimulation of the LDL receptor-mediated lipoprotein catabolism. |
List of Excipients |
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Bezafibrate 200 mg Film-coated Tablets contain the following excipients: Tablet core excipients: Silica, colloidal anhydrous Film coat excipients: Hypromellose |
Bezafibrate 200 mg Film-coated Tablets are available in either: -
Not all pack sizes may be marketed.
Generics [UK] Ltd t/a Mylan, Station Close, Potters Bar, Herts, EN6 1TL
PL 04569/0390
26 October 1999 / 8 April 2005
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