Atorvastatin Malta - English - Medicines Authority

atorvastatin

accord healthcare limited - atorvastatin calcium trihydrate - film-coated tablet - atorvastatin calcium trihydrate 80 mg - lipid modifying agents

Atorvastatin Malta - English - Medicines Authority

atorvastatin

accord healthcare limited - atorvastatin calcium trihydrate - film-coated tablet - atorvastatin calcium trihydrate 10 mg - lipid modifying agents

Atorvastatin Malta - English - Medicines Authority

atorvastatin

accord healthcare limited - atorvastatin calcium trihydrate - film-coated tablet - atorvastatin calcium trihydrate 20 mg - lipid modifying agents

EZETIMIBE/ATORVASTATIN GH 10/40 ezetimibe and atorvastatin (as calcium trihydrate) 10 mg/40 mg tablets blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

ezetimibe/atorvastatin gh 10/40 ezetimibe and atorvastatin (as calcium trihydrate) 10 mg/40 mg tablets blister pack

lupin australia pty limited - ezetimibe, quantity: 10 mg; atorvastatin calcium trihydrate, quantity: 41.363 mg (equivalent: atorvastatin, qty 40 mg) - tablet, film coated - excipient ingredients: colloidal anhydrous silica; microcrystalline cellulose; sodium lauryl sulfate; sodium stearylfumarate; lactose; calcium carbonate; povidone; crospovidone; lactose monohydrate; hyprolose; titanium dioxide; purified talc; xanthan gum; polyvinyl alcohol; lecithin - prevention of cardiovascular disease ezetimibe/atorvastatin is indicated in patients with coronary heart disease (chd) and a history of acute coronary syndrome (acs) taking their maximum tolerated dose of atorvastatin and in need of additional lowering of ldl-c in the expectation of a modest further reduction in the risk of cardiovascular events following at least one year of therapy,primary hypercholesterolaemia ezetimibe/atorvastatin is indicated as adjunctive therapy to diet in patients with primary (heterozygous familial and non-familial) hypercholesterolaemia where use of a combination product is appropriate in those patients: ? not appropriately controlled with atorvastatin or ezetimibe alone; or ? already treated with atorvastatin and ezetimibe.,homozygous familial hypercholesterolaemia (hofh) ezetimibe/atorvastatin is indicated in patients with hofh. patients may also receive adjunctive treatments (eg. ldl apheresis).

Ezetimibe Sandoz New Zealand - English - Medsafe (Medicines Safety Authority)

ezetimibe sandoz

sandoz new zealand limited - ezetimibe 10mg;   - tablet - 10 mg - active: ezetimibe 10mg   excipient: croscarmellose sodium hypromellose lactose monohydrate magnesium stearate microcrystalline cellulose sodium laurilsulfate - ezetimibe sandoz administered with an hmg-coa reductase inhibitor (statin) or alone, is indicated as adjunctive therapy to diet for the reduction of elevated total cholesterol (total-c), low-density lipoprotein cholesterol (ldl-c), apolipoprotein b (apo b), and triglycerides (tg) and to increase high-density lipoprotein cholesterol (hdl-c) in adult and adolescent (10 to 17 years of age) patients with primary (heterozygous familial and non-familial) hypercholesterolaemia.

ATOZET ezetimibe/atorvastatin 10mg/40mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

atozet ezetimibe/atorvastatin 10mg/40mg tablet blister pack

organon pharma pty ltd - ezetimibe, quantity: 10 mg; atorvastatin calcium trihydrate, quantity: 43.4 mg (equivalent: atorvastatin, qty 40 mg) - tablet, multilayer - excipient ingredients: hyprolose; lactose monohydrate; croscarmellose sodium; silicon dioxide; magnesium stearate; microcrystalline cellulose; povidone; polysorbate 80; sodium lauryl sulfate; calcium carbonate; titanium dioxide; macrogol 8000; hypromellose; purified talc - prevention of cardiovascular disease atozet is indicated in patients with coronary heart disease (chd) and a history of acute coronary syndrome (acs) taking their maximum tolerated dose of atorvastatin and in need of additional lowering of ldl-c in the expectation of a modest further reduction in the risk of cardiovascular events following at least one year of therapy (see clinical trials). primary hypercholesterolaemia atozet is indicated as adjunctive therapy to diet in patients with primary (heterozygous familial and non-familial) hypercholesterolaemia where use of a combination product is appropriate in those patients: - not appropriately controlled with atorvastatin or ezetimibe alone; - or already treated with atorvastatin and ezetimibe homozygous familial hypercholesterolaemia (hofh) atozet is indicated in patients with hofh. patients may also receive adjunctive treatments (e.g. ldl apheresis).

Atorvastatin Basics 30 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin basics 30 mg film-coated tablets

basics gmbh hemmelrather weg 201 51377 leverkusen, germany - atorvastatin calcium, trihydrate - film-coated tablet - atorvastatin calcium trihydrate 30 mg - lipid modifying agents

Atorvastatin Basics 60 mg film-coated tablets Malta - English - Medicines Authority

atorvastatin basics 60 mg film-coated tablets

basics gmbh hemmelrather weg 201 51377 leverkusen, germany - atorvastatin calcium, trihydrate - film-coated tablet - atorvastatin calcium trihydrate 60 mg - lipid modifying agents

Atorvastatin Krka Coated Tablets 10mg Malta - English - Medicines Authority

atorvastatin krka coated tablets 10mg

krka dd novo mesto Šmarješka cesta 6, 8501 novo mesto, slovenia - atorvastatin - film-coated tablet - atorvastatin 10 mg - lipid modifying agents

Atorvastatin Krka Coated Tablets 20mg Malta - English - Medicines Authority

atorvastatin krka coated tablets 20mg

krka dd novo mesto Šmarješka cesta 6, 8501 novo mesto, slovenia - atorvastatin - film-coated tablet - atorvastatin 20 mg - lipid modifying agents