APO-LURASIDONE lurasidone hydrochloride 80 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

apo-lurasidone lurasidone hydrochloride 80 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - lurasidone hydrochloride, quantity: 80 mg - tablet, film coated - excipient ingredients: hypromellose; maize starch; mannitol; croscarmellose sodium; magnesium stearate; titanium dioxide; macrogol 8000; iron oxide yellow; indigo carmine aluminium lake - apo-lurasidone is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

APO-LURASIDONE lurasidone hydrochloride 40 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

apo-lurasidone lurasidone hydrochloride 40 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: hypromellose; maize starch; mannitol; croscarmellose sodium; magnesium stearate; titanium dioxide; macrogol 8000 - apo-lurasidone is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

APO-LURASIDONE lurasidone hydrochloride 20 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

apo-lurasidone lurasidone hydrochloride 20 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: hypromellose; maize starch; mannitol; croscarmellose sodium; magnesium stearate; titanium dioxide; macrogol 8000 - apo- lurasidone is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE SANDOZ lurasidone hydrochloride 80 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

lurasidone sandoz lurasidone hydrochloride 80 mg film-coated tablet blister pack

sandoz pty ltd - lurasidone hydrochloride, quantity: 80 mg - tablet, film coated - excipient ingredients: hypromellose; maize starch; mannitol; croscarmellose sodium; magnesium stearate; titanium dioxide; macrogol 8000; iron oxide yellow; indigo carmine aluminium lake - lurasidone sandoz is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE SANDOZ lurasidone hydrochloride 40 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

lurasidone sandoz lurasidone hydrochloride 40 mg film-coated tablet blister pack

sandoz pty ltd - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: hypromellose; maize starch; mannitol; croscarmellose sodium; magnesium stearate; titanium dioxide; macrogol 8000 - lurasidone sandoz is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE LUPIN lurasidone hydrochloride 20 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

lurasidone lupin lurasidone hydrochloride 20 mg film-coated tablet blister pack

lupin australia pty limited - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: hypromellose; mannitol; magnesium stearate; croscarmellose sodium; titanium dioxide; macrogol 6000 - lurasidone lupin is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE LUPIN lurasidone hydrochloride 40 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

lurasidone lupin lurasidone hydrochloride 40 mg film-coated tablet blister pack

lupin australia pty limited - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: hypromellose; croscarmellose sodium; magnesium stearate; mannitol; titanium dioxide; macrogol 6000 - lurasidone lupin is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE LUPIN lurasidone hydrochloride 80 mg film-coated tablet blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

lurasidone lupin lurasidone hydrochloride 80 mg film-coated tablet blister pack

lupin australia pty limited - lurasidone hydrochloride, quantity: 80 mg - tablet, film coated - excipient ingredients: mannitol; hypromellose; magnesium stearate; croscarmellose sodium; titanium dioxide; iron oxide yellow; macrogol 6000; indigo carmine aluminium lake - lurasidone lupin is indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURASIDONE HYDROCHLORIDE tablet, film coated Stati Uniti - Ingliż - NLM (National Library of Medicine)

lurasidone hydrochloride tablet, film coated

alembic pharmaceuticals inc. - lurasidone hydrochloride (unii: o0p4i5851i) (lurasidone - unii:22ic88528t) -  lurasidone hydrochloride tablets are indicated for: - monotherapy treatment of adult and pediatric patients (10 to 17 years) with major depressive episode associated with bipolar i disorder (bipolar depression) [see clinical studies (14.2)] . - adjunctive treatment with lithium or valproate in adult patients with major depressive episode associated with bipolar i disorder (bipolar depression) [see clinical studies (14.2)]. - known hypersensitivity to lurasidone hcl or any components in the formulation. angioedema has been observed with lurasidone [see adverse reactions (6.1)]. - strong cyp3a4 inhibitors (e.g., ketoconazole, clarithromycin, ritonavir, voriconazole, mibefradil, etc.) [see drug interactions (7.1)] . - strong cyp3a4 inducers (e.g., rifampin, avasimibe, st. john’s wort, phenytoin, carbamazepine, etc.) [see drug interactions (7.1)]. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to lurasidone hydrochloride during pregnancy. for

LURASIDONE HYDROCHLORIDE tablet, film coated Stati Uniti - Ingliż - NLM (National Library of Medicine)

lurasidone hydrochloride tablet, film coated

alembic pharmaceuticals limited - lurasidone hydrochloride (unii: o0p4i5851i) (lurasidone - unii:22ic88528t) -  lurasidone hydrochloride tablets are indicated for: - monotherapy treatment of adult and pediatric patients (10 to 17 years) with major depressive episode associated with bipolar i disorder (bipolar depression) [see clinical studies (14.2)] . - adjunctive treatment with lithium or valproate in adult patients with major depressive episode associated with bipolar i disorder (bipolar depression) [see clinical studies (14.2)]. - known hypersensitivity to lurasidone hcl or any components in the formulation. angioedema has been observed with lurasidone [see adverse reactions (6.1)]. - strong cyp3a4 inhibitors (e.g., ketoconazole, clarithromycin, ritonavir, voriconazole, mibefradil, etc.) [see drug interactions (7.1)] . - strong cyp3a4 inducers (e.g., rifampin, avasimibe, st. john’s wort, phenytoin, carbamazepine, etc.) [see drug interactions (7.1)]. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to lurasidone hydrochloride during pregnancy. for