New Zealand - English - Medsafe (Medicines Safety Authority)

actavis new zealand limited - alprazolam 2mg;   - tablet - 2 mg - active: alprazolam 2mg   excipient: colloidal silicon dioxide docusate sodium lactose magnesium stearate maize starch microcrystalline cellulose povidone sodium benzoate sodium starch glycolate

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 100mg; lamotrigine 100mg - chewable/dispersible tablet - 100 mg - active: lamotrigine 100mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium active: lamotrigine 100mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 200mg - chewable/dispersible tablet - 200 mg - active: lamotrigine 200mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 25mg; lamotrigine 25mg - chewable/dispersible tablet - 25 mg - active: lamotrigine 25mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium active: lamotrigine 25mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 2mg - chewable/dispersible tablet - 2 mg - active: lamotrigine 2mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 50mg; lamotrigine 50mg - chewable/dispersible tablet - 50 mg - active: lamotrigine 50mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium active: lamotrigine 50mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - lamotrigine 5mg; lamotrigine 5mg - chewable/dispersible tablet - 5 mg - active: lamotrigine 5mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium active: lamotrigine 5mg excipient: colloidal silicon dioxide as silica - colloidal anhydrous croscarmellose sodium magnesium stearate mannitol microcrystalline cellulose povidone purified talc purified water ribes nigrum saccharin sodium - epilepsy adults (over 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures, including tonic-clonic seizures and the seizures associated with lennox-gastaut syndrome. children (2 to 12 years of age) arrow - lamotrigine is indicated as adjunctive therapy in the treatment of epilepsy, for partial seizures and generalised seizures including tonic-clonic seizures and the seizures associated with lennox-gaustaut syndrome. bipolar disorder (adults 18 years of age and over) arrow - lamotrigine is indicated for the prevention of mood episodes in patients with bipolar disorder, predominantly by preventing depressive episodes.

New Zealand - English - Medsafe (Medicines Safety Authority)

teva pharma (new zealand) limited - latanoprost 0.05 mg/ml; timolol maleate 6.8 mg/ml equivalent to timolol 5 mg/ml - eye drops, solution - 0.05mg/ml, 5mg/ml - active: latanoprost 0.05 mg/ml timolol maleate 6.8 mg/ml equivalent to timolol 5 mg/ml excipient: benzalkonium chloride dibasic sodium phosphate hydrochloric acid monobasic sodium phosphate monohydrate sodium chloride sodium hydroxide water for injection - reduction of intraocular pressure (iop) in patients with open angle glaucoma and ocular hypertension who are insufficiently responsive to topical beta-blockers or prostaglandin analogues. arrow-lattim should not be used to initiate therapy.

New Zealand - English - Medsafe (Medicines Safety Authority)

actavis new zealand limited - metformin hydrochloride 1000mg;  ;   - coated tablet - 1000 mg - active: metformin hydrochloride 1000mg     excipient: magnesium stearate opadry clear oy-29020 povidone water - -treatment of type 2 diabetes mellitus in adults, particularly in overweight patients, when dietary management and exercise alone does not result in adequate glycaemic control. -metformin may be used as initial treatment or in sulfonylurea failures either alone or in combination with a sulfonylurea and other oral agents. - adjuvant therapy in insulin dependent diabetes especially if overweight.

New Zealand - English - Medsafe (Medicines Safety Authority)

actavis new zealand limited - metformin hydrochloride 250mg - coated tablet - 250 mg - active: metformin hydrochloride 250mg excipient: magnesium stearate opadry clear oy-29020 povidone water