Amlodipine Besilate Viatris 5 mg tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

amlodipine besilate viatris 5 mg tabl.

viatris gx bv-srl - amlodipine besilate 6,94 mg - eq. amlodipine 5 mg - tablet - 5 mg - amlodipine besilate - amlodipine

Amlodipine Besilate Viatris 10 mg tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

amlodipine besilate viatris 10 mg tabl.

viatris gx bv-srl - amlodipine besilate 13,88 mg - eq. amlodipine 10 mg - tablet - 10 mg - amlodipine besilate - amlodipine

APO-OLMESARTAN/AMLODIPINE/HCTZ 40/10/12.5 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/12.5 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

apo-olmesartan/amlodipine/hctz 40/10/12.5 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/12.5 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - amlodipine besilate, quantity: 13.9 mg; hydrochlorothiazide, quantity: 12.5 mg; olmesartan medoxomil, quantity: 40 mg - tablet, film coated - excipient ingredients: lactose monohydrate; magnesium stearate; povidone; pregelatinised maize starch; silicified microcrystalline cellulose; isopropyl alcohol; titanium dioxide; purified talc; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350 - apo-olmesartan/amlodipine/hctz 40/10/12.5 mg is indicated for the treatment of hypertension, either as replacement for olmesartan medoxomil, amlodipine and hydrochlorothiazide being already taken as separate tablets or as add-on therapy where a patient's blood pressure is not controlled on a dual combination. this fixed dose combination is not indicated for initial therapy.

APO-OLMESARTAN/AMLODIPINE/HCTZ 40/10/25 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/25 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

apo-olmesartan/amlodipine/hctz 40/10/25 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/25 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - amlodipine besilate, quantity: 13.9 mg; hydrochlorothiazide, quantity: 25 mg; olmesartan medoxomil, quantity: 40 mg - tablet, film coated - excipient ingredients: isopropyl alcohol; silicified microcrystalline cellulose; povidone; lactose monohydrate; pregelatinised maize starch; magnesium stearate; titanium dioxide; purified talc; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350 - apo-olmesartan/amlodipine/hctz 40/10/25 mg is indicated for the treatment of hypertension, either as replacement for olmesartan medoxomil, amlodipine and hydrochlorothiazide being already taken as separate tablets or as add-on therapy where a patient's blood pressure is not controlled on a dual combination. this fixed dose combination is not indicated for initial therapy.

APO-Perindopril Arginine/Amlodipine 5/10 perindopril arginine 5 mg and amlodipine (as besilate) 10 mg uncoated tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

apo-perindopril arginine/amlodipine 5/10 perindopril arginine 5 mg and amlodipine (as besilate) 10 mg uncoated tablet bottle

arrotex pharmaceuticals pty ltd - amlodipine besilate, quantity: 13.87 mg (equivalent: amlodipine, qty 10 mg); perindopril arginine, quantity: 5 mg - tablet - excipient ingredients: colloidal anhydrous silica; croscarmellose sodium; microcrystalline cellulose; magnesium stearate - perindopril arginine and amlodipine combination tablet is indicated as substitution therapy for the treatment of hypertension and/or stable coronary heart disease in patients already controlled with separate doses of perindopril and amlodipine, given concurrently at the same dose level. treatment should not be initiated with this combination.

Auro-Amlodipine 5 mg Namibia - English - Namibia Medicines Regulatory Council

auro-amlodipine 5 mg

aurobindo pharma (pty) ltd - amlodipine besilate - tablet - each tablet contains amlodipine besilate equivalent to amlodipine 5,0 mg

Auro-Amlodipine 10 mg Namibia - English - Namibia Medicines Regulatory Council

auro-amlodipine 10 mg

aurobindo pharma (pty) ltd - amlodipine besilate - tablet - each tablet contains amlodipine besilate equivalent to amlodipine 10,0 mg

Exforge HCT New Zealand - English - Medsafe (Medicines Safety Authority)

exforge hct

novartis new zealand ltd - amlodipine besilate 6.94mg equivalent to amlodipine 5 mg;  ; hydrochlorothiazide 12.5mg;  ;  ; valsartan 160mg;  ;  ;  ;   - film coated tablet - 5/160/12.5mg - active: amlodipine besilate 6.94mg equivalent to amlodipine 5 mg   hydrochlorothiazide 12.5mg     valsartan 160mg         excipient: colloidal silicon dioxide crospovidone magnesium stearate microcrystalline cellulose opadry white 00f18296 - exforge hct is indicated only as substitution therapy for the treatment of hypertension in patients whose blood pressure is already adequately controlled on the triple combination of amlodipine, valsartan and hydrochlorothiazide taken either as three single component formulations or as dual component formulation with a single component formulation, all components at the same dose level. treatment should not be initiated with these fixed-dose combinations.

Exforge HCT New Zealand - English - Medsafe (Medicines Safety Authority)

exforge hct

novartis new zealand ltd - amlodipine besilate 6.94mg equivalent to amlodipine 5 mg;  ; hydrochlorothiazide 25mg;  ;  ; valsartan 160mg;  ;  ;  ;   - film coated tablet - 5/160/25mg - active: amlodipine besilate 6.94mg equivalent to amlodipine 5 mg   hydrochlorothiazide 25mg     valsartan 160mg         excipient: colloidal silicon dioxide crospovidone magnesium stearate microcrystalline cellulose opadry white 00f18296 opadry yellow 00f12951 - exforge hct is indicated only as substitution therapy for the treatment of hypertension in patients whose blood pressure is already adequately controlled on the triple combination of amlodipine, valsartan and hydrochlorothiazide taken either as three single component formulations or as dual component formulation with a single component formulation, all components at the same dose level. treatment should not be initiated with these fixed-dose combinations.

ALKEM AMLODIPINE amlodipine (as besilate) 10 mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

alkem amlodipine amlodipine (as besilate) 10 mg tablet bottle

pharmacor pty ltd - amlodipine besilate, quantity: 13.87 mg (equivalent: amlodipine, qty 10 mg) - tablet - excipient ingredients: magnesium stearate; silicon dioxide; calcium phosphate; microcrystalline cellulose; sodium starch glycollate type a - hypertension,alkem amlodipine is indicated for the first line treatment of hypertension and can be used as the sole agent to control blood pressure in the majority of patients. patients not adequately controlled on a single antihypertensive agent may benefit from the addition of alkem amlodipine, which has been used in combination with a thiazide diuretic, beta adrenoceptor blocking agent or an angiotensin-converting enzyme inhibitor.,angina,alkem amlodipine is indicated for the first line treatment of chronic stable angina. alkem amlodipine may be used alone, as monotherapy or in combination with other antianginal drugs.