DSM Nutritional Products Australia Pty Ltd - risultati della ricerca

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

ronozyme a (l)

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

ronozyme wx (ct)

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

ronozyme wx (l)

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

ronozyme p (l)

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

roxazyme g2 liquid multienzyme complex for poultry

Australia - inglese - APVMA (Australian Pesticides and Veterinary Medicines Authority)

roxazyme g multienzyme complex for poultry

Australia - inglese - Department of Health (Therapeutic Goods Administration)

sandoz venlafaxine xr venlafaxine (as hydrochloride) 150 mg modified release capsule blister pack

alembic pharmaceuticals australia pty ltd - venlafaxine hydrochloride, quantity: 169.8 mg (equivalent: venlafaxine, qty 150 mg) - capsule, modified release - excipient ingredients: gelatin; ethylcellulose; sunset yellow fcf; povidone; magnesium stearate; microcrystalline cellulose; brilliant blue fcf; copovidone; allura red ac; purified talc; colloidal anhydrous silica; titanium dioxide; propylene glycol; ethanol; isopropyl alcohol; shellac; tert-butyl alcohol; sodium hydroxide - sandoz venlafaxine xr is indicated for the treatment of: - major depression, including prevention of relapse and recurrence where appropriate; - generalised anxiety disorder; - social anxiety disorder; panic disorder, including prevention of relapse.

Australia - inglese - Department of Health (Therapeutic Goods Administration)

sandoz venlafaxine xr venlafaxine (as hydrochloride) 75 mg modified release capsule blister pack

alembic pharmaceuticals australia pty ltd - venlafaxine hydrochloride, quantity: 84.9 mg (equivalent: venlafaxine, qty 75 mg) - capsule, modified release - excipient ingredients: iron oxide black; colloidal anhydrous silica; ethylcellulose; iron oxide red; magnesium stearate; microcrystalline cellulose; povidone; purified talc; titanium dioxide; gelatin; copovidone; propylene glycol; butan-1-ol; isopropyl alcohol; purified water; shellac; ethanol absolute; ammonia - sandoz venlafaxine xr is indicated for the treatment of: - major depression, including prevention of relapse and recurrence where appropriate; - generalised anxiety disorder; - social anxiety disorder; panic disorder, including prevention of relapse.

Australia - inglese - Department of Health (Therapeutic Goods Administration)

sequase xr quetiapine (as fumarate) 400 mg modified release tablet blister pack

luye pharma australia pty ltd - quetiapine fumarate, quantity: 460.5 mg (equivalent: quetiapine, qty 400 mg) - tablet, modified release - excipient ingredients: lactose monohydrate; microcrystalline cellulose; sodium citrate dihydrate; hypromellose; magnesium stearate; macrogol 400; titanium dioxide - sequase xr is indicated for: bipolar disorder - maintenance treatment of bipolar i disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes - treatment of depressive episodes associated with bipolar disorder (see dosage and administration) - treatment of acute mania associated with bipolar i disorder as monotherapy or in combination with lithium or sodium valproate. efficacy of sequase xr in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine ir. schizophrenia: treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder: treatment of recurrent major depressive disorder (mdd) in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder: treatment of generalised anxiety disorder (gad).

Australia - inglese - Department of Health (Therapeutic Goods Administration)

sequase xr quetiapine (as fumarate) 300 mg modified release tablet blister pack

luye pharma australia pty ltd - quetiapine fumarate, quantity: 345.38 mg - tablet, modified release - excipient ingredients: lactose monohydrate; microcrystalline cellulose; sodium citrate dihydrate; hypromellose; magnesium stearate; macrogol 400; titanium dioxide; iron oxide yellow - sequase xr is indicated for: bipolar disorder - maintenance treatment of bipolar i disorder, as monotherapy or in combination with lithium or sodium valproate, for the prevention of relapse/recurrence of manic, depressive or mixed episodes - treatment of depressive episodes associated with bipolar disorder (see dosage and administration) - treatment of acute mania associated with bipolar i disorder as monotherapy or in combination with lithium or sodium valproate. efficacy of sequase xr in the treatment of bipolar disorder indications was established in part, on the basis of extrapolation from the established effectiveness of quetiapine ir. schizophrenia: treatment of schizophrenia, prevention of relapse and maintenance of clinical improvement during continuation therapy. major depressive disorder: treatment of recurrent major depressive disorder (mdd) in patients who are intolerant of, or who have an inadequate response to alternative therapies. generalised anxiety disorder: treatment of generalised anxiety disorder (gad).