SACVAL 50 Tablet Kenya - angol - Pharmacy and Poisons Board

sacval 50 tablet

pharmaken ltd p.o box 95625-80106 - sacubitril 24mg / valsartan 26mg - tablet - sacubitril 24mg / valsartan 26mg - valsartan and sacubitril

SECUTRIL-VT 100 Tablet Kenya - angol - Pharmacy and Poisons Board

secutril-vt 100 tablet

innocia lifesciences pvt ltd innocia lifesciences pvt ltd - sacubitril 49mg and valsartan 51mg tablets - tablet - sacubitril 49mg and valsartan 51mg tablets - valsartan and sacubitril

SECUTRIL-VT 200 Tablet Kenya - angol - Pharmacy and Poisons Board

secutril-vt 200 tablet

innocia lifesciences pvt ltd innocia lifesciences pvt ltd - sacubitril 97mg and valsartan 103mg tablets - tablet - sacubitril 97mg and valsartan 103mg tablets - valsartan and sacubitril

SECUTRIL-VT 50 Tablet Kenya - angol - Pharmacy and Poisons Board

secutril-vt 50 tablet

innocia lifesciences pvt ltd innocia lifesciences pvt ltd - sacubitril 24mg and valsartan 26mg tablets - tablet - sacubitril 24mg and valsartan 26mg tablets - valsartan and sacubitril

SACUVAN 49/51 Film-Coated Tablet Kenya - angol - Pharmacy and Poisons Board

sacuvan 49/51 film-coated tablet

sacubitril valsartan sodium on colloidal silicon… - film-coated tablet - sacubitril 49mg valsartan sodium 51mg on… - valsartan and sacubitril

VALTRESTO sacubitril/valsartan 24/26 mg film-coated tablet bottle pack Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

valtresto sacubitril/valsartan 24/26 mg film-coated tablet bottle pack

pharmacor pty ltd - valsartan, quantity: 25.7 mg; sacubitril, quantity: 24.3 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; sodium starch glycollate type a; purified talc; hyprolose; magnesium stearate; microcrystalline cellulose; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 4000; iron oxide black - valtresto is indicated in adult patients for the treatment of chronic heart failure (nyha class ii-iv) with reduced ejection fraction.

Entresto 24/26 Új-Zéland - angol - Medsafe (Medicines Safety Authority)

entresto 24/26

novartis new zealand ltd - sacubitril/valsartan 50mg (as sodium hydrate complex, contains 24.3 mg sacubitril and 25.7 mg valsartan);  ;   - film coated tablet - 24.3 mg/25.7 mg - active: sacubitril/valsartan 50mg (as sodium hydrate complex, contains 24.3 mg sacubitril and 25.7 mg valsartan)     excipient: colloidal silicon dioxide crospovidone hyprolose basic coating premix, white basic coating premix, red basic coating premix, black magnesium stearate microcrystalline cellulose purified talc purified water - entresto is indicated in adult patients with chronic heart failure (nyha class ii-iv). benefits are most clearly evident in patients with left ventricular ejection fraction (lvef) below normal. lvef is a variable measure, so use clinical judgment in deciding whom to treat

Entresto 49/51 Új-Zéland - angol - Medsafe (Medicines Safety Authority)

entresto 49/51

novartis new zealand ltd - sacubitril/valsartan 100mg (as sodium hydrate complex, contains 48.6 mg sacubitril and 51.4 mg valsartan);  ;   - film coated tablet - 48.6 mg/51.4 mg - active: sacubitril/valsartan 100mg (as sodium hydrate complex, contains 48.6 mg sacubitril and 51.4 mg valsartan)     excipient: colloidal silicon dioxide crospovidone hyprolose basic coating premix, white basic coating premix, yellow basic coating premix, red magnesium stearate microcrystalline cellulose purified talc purified water - entresto is indicated in adult patients with chronic heart failure (nyha class ii-iv). benefits are most clearly evident in patients with left ventricular ejection fraction (lvef) below normal. lvef is a variable measure, so use clinical judgment in deciding whom to treat

Entresto 97/103 Új-Zéland - angol - Medsafe (Medicines Safety Authority)

entresto 97/103

novartis new zealand ltd - sacubitril/valsartan 200mg (as sodium hydrate complex, contains 97.2 mg sacubitril and 102.8 mg valsartan);  ;   - film coated tablet - 97.2 mg/102.8 mg - active: sacubitril/valsartan 200mg (as sodium hydrate complex, contains 97.2 mg sacubitril and 102.8 mg valsartan)     excipient: colloidal silicon dioxide crospovidone hyprolose basic coating mixture, white basic coating mixture, red basic coating mixture, black magnesium stearate microcrystalline cellulose purified talc purified water - entresto is indicated in adult patients with chronic heart failure (nyha class ii-iv). benefits are most clearly evident in patients with left ventricular ejection fraction (lvef) below normal. lvef is a variable measure, so use clinical judgment in deciding whom to treat

Entresto Európai Unió - angol - EMA (European Medicines Agency)

entresto

novartis europharm limited - sacubitril, valsartan - heart failure - angiotensin ii antagonists, other combinations, agents acting on the renin-angiotensin system - paediatric heart failureentresto is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction.adult heart failureentresto is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction.