VALTRESTO sacubitril/valsartan 97/103 mg film-coated tablet bottle pack Australia - English - Department of Health (Therapeutic Goods Administration)

valtresto sacubitril/valsartan 97/103 mg film-coated tablet bottle pack

pharmacor pty ltd - sacubitril, quantity: 97.2 mg; valsartan, quantity: 102.8 mg - tablet, film coated - excipient ingredients: hyprolose; magnesium stearate; purified talc; microcrystalline cellulose; sodium starch glycollate type a; colloidal anhydrous silica; 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.

PHARMACOR SACUBITRIL VALSARTAN sacubitril/valsartan 49/51mg film-coated tablet bottle pack Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor sacubitril valsartan sacubitril/valsartan 49/51mg film-coated tablet bottle pack

pharmacor pty ltd - sacubitril, quantity: 48.6 mg; valsartan, quantity: 51.4 mg - tablet, film coated - excipient ingredients: hyprolose; microcrystalline cellulose; colloidal anhydrous silica; sodium starch glycollate type a; purified talc; magnesium stearate; titanium dioxide; hypromellose; iron oxide yellow; macrogol 4000 - pharmacor sacubitril/valsartan is indicated in adult patients for the treatment of chronic heart failure (nyha class ii-iv) with reduced ejection fraction.

VALTRESTO sacubitril/valsartan 49/51 mg film-coated tablet bottle pack Australia - English - Department of Health (Therapeutic Goods Administration)

valtresto sacubitril/valsartan 49/51 mg film-coated tablet bottle pack

pharmacor pty ltd - sacubitril, quantity: 48.6 mg; valsartan, quantity: 51.4 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; magnesium stearate; sodium starch glycollate type a; purified talc; hyprolose; microcrystalline cellulose; titanium dioxide; hypromellose; iron oxide yellow; macrogol 4000 - valtresto is indicated in adult patients for the treatment of chronic heart failure (nyha class ii-iv) with reduced ejection fraction.