GIOTRIF afatinib 50 mg (as dimaleate) film coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

giotrif afatinib 50 mg (as dimaleate) film coated tablet blister pack

boehringer ingelheim pty ltd - afatinib dimaleate, quantity: 73.9 mg - tablet, film coated - excipient ingredients: purified talc; polysorbate 80; indigo carmine aluminium lake; colloidal anhydrous silica; magnesium stearate; lactose monohydrate; macrogol 400; hypromellose; microcrystalline cellulose; titanium dioxide; crospovidone - giotrif is indicated as monotherapy for the treatment of adult patients with:,? locally advanced or metastatic non-squamous non-small cell carcinoma of the lung, either as first line therapy or after failure of cytotoxic chemotherapy. tumours must have activating epidermal growth factor receptor (egfr) mutations.,? locally advanced or metastatic squamous non-small cell carcinoma of the lung progressing on or after platinum-based chemotherapy.

GIOTRIF afatinib 30 mg (as dimaleate) film coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

giotrif afatinib 30 mg (as dimaleate) film coated tablet blister pack

boehringer ingelheim pty ltd - afatinib dimaleate, quantity: 44.34 mg - tablet, film coated - excipient ingredients: crospovidone; titanium dioxide; polysorbate 80; lactose monohydrate; macrogol 400; colloidal anhydrous silica; microcrystalline cellulose; hypromellose; magnesium stearate; purified talc; indigo carmine aluminium lake - giotrif is indicated as monotherapy for the treatment of adult patients with:,? locally advanced or metastatic non-squamous non-small cell carcinoma of the lung, either as first line therapy or after failure of cytotoxic chemotherapy. tumours must have activating epidermal growth factor receptor (egfr) mutations.,? locally advanced or metastatic squamous non-small cell carcinoma of the lung progressing on or after platinum-based chemotherapy.

GIOTRIF afatinib 40 mg (as dimaleate) film coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

giotrif afatinib 40 mg (as dimaleate) film coated tablet blister pack

boehringer ingelheim pty ltd - afatinib dimaleate, quantity: 59.12 mg - tablet, film coated - excipient ingredients: titanium dioxide; macrogol 400; purified talc; crospovidone; lactose monohydrate; hypromellose; microcrystalline cellulose; indigo carmine aluminium lake; colloidal anhydrous silica; polysorbate 80; magnesium stearate - giotrif is indicated as monotherapy for the treatment of adult patients with:,? locally advanced or metastatic non-squamous non-small cell carcinoma of the lung, either as first line therapy or after failure of cytotoxic chemotherapy. tumours must have activating epidermal growth factor receptor (egfr) mutations.,? locally advanced or metastatic squamous non-small cell carcinoma of the lung progressing on or after platinum-based chemotherapy.

GIOTRIF afatinib 20 mg (as dimaleate) film coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

giotrif afatinib 20 mg (as dimaleate) film coated tablet blister pack

boehringer ingelheim pty ltd - afatinib dimaleate, quantity: 29.56 mg - tablet, film coated - excipient ingredients: lactose monohydrate; polysorbate 80; magnesium stearate; macrogol 400; titanium dioxide; crospovidone; microcrystalline cellulose; colloidal anhydrous silica; hypromellose; purified talc - giotrif is indicated as monotherapy for the treatment of adult patients with:,? locally advanced or metastatic non-squamous non-small cell carcinoma of the lung, either as first line therapy or after failure of cytotoxic chemotherapy. tumours must have activating epidermal growth factor receptor (egfr) mutations.,? locally advanced or metastatic squamous non-small cell carcinoma of the lung progressing on or after platinum-based chemotherapy.

FINPRO finasteride 5 mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

finpro finasteride 5 mg film-coated tablet blister pack

dr reddys laboratories australia pty ltd - finasteride, quantity: 5 mg - tablet, film coated - excipient ingredients: lactose monohydrate; pregelatinised maize starch; microcrystalline cellulose; sodium starch glycollate type a; magnesium stearate; docusate sodium; titanium dioxide; hypromellose; indigo carmine aluminium lake; macrogol 400 - treatment of patients with symptomatic benign prostatic hyperplasia (bph) with an enlarged prostate.

DONEPEZIL SANDOZ donepezil hydrochloride (as monohydrate) 5mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

donepezil sandoz donepezil hydrochloride (as monohydrate) 5mg film-coated tablet blister pack

sandoz pty ltd - donepezil hydrochloride monohydrate, quantity: 5.22 mg (equivalent: donepezil hydrochloride, qty 5 mg) - tablet, film coated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; magnesium stearate; maize starch; titanium dioxide; purified talc; polyvinyl alcohol; macrogol 3350; lecithin - treatment of mild, moderate and severe alzheimer's disease.

DONEPEZIL SANDOZ donepezil hydrochloride (as monohydrate) 10mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

donepezil sandoz donepezil hydrochloride (as monohydrate) 10mg film-coated tablet blister pack

sandoz pty ltd - donepezil hydrochloride monohydrate, quantity: 10.43 mg (equivalent: donepezil hydrochloride, qty 10 ) - tablet, film coated - excipient ingredients: lactose monohydrate; magnesium stearate; maize starch; microcrystalline cellulose; titanium dioxide; purified talc; iron oxide yellow; polyvinyl alcohol; macrogol 3350; lecithin - treatment of mild, moderate and severe alzheimer's disease.

COZAVAN losartan potassium 25 mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

cozavan losartan potassium 25 mg film-coated tablet blister pack

alphapharm pty ltd - losartan potassium, quantity: 25 mg - tablet, film coated - excipient ingredients: magnesium stearate; pregelatinised maize starch; lactose monohydrate; microcrystalline cellulose; titanium dioxide; hypromellose; hyprolose - hypertension: cozavan is indicated for the treatment of hypertension. it may be used alone or in combination with other antihypertensive agents (e.g. thiazide diuretics). renal protection in type 2 diabetic patients with proteinuria: cozavan is indicated to delay the progression of renal disease in hypertensive type 2 diabetics with proteinuria, defined as urinary albumin to creatinine ratio greater than or equal to 300mg/g.

COZAVAN losartan potassium 50 mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

cozavan losartan potassium 50 mg film-coated tablet blister pack

alphapharm pty ltd - losartan potassium, quantity: 50 mg - tablet, film coated - excipient ingredients: lactose monohydrate; pregelatinised maize starch; microcrystalline cellulose; magnesium stearate; titanium dioxide; hypromellose; hyprolose - hypertension: cozavan is indicated for the treatment of hypertension. it may be used alone or in combination with other antihypertensive agents (e.g. thiazide diuretics). renal protection in type 2 diabetic patients with proteinuria: cozavan is indicated to delay the progression of renal disease in hypertensive type 2 diabetics with proteinuria, defined as urinary albumin to creatinine ratio greater than or equal to 300mg/g.

ZALDIAR  tramadol hydrochloride / paracetamol 37.5 mg/ 325 mg film coated tablets blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

zaldiar tramadol hydrochloride / paracetamol 37.5 mg/ 325 mg film coated tablets blister pack

aspen pharmacare australia pty ltd - paracetamol, quantity: 325 mg; tramadol hydrochloride, quantity: 37.5 mg - tablet, film coated - excipient ingredients: powdered cellulose; magnesium stearate; macrogol 6000; sodium starch glycollate type a; titanium dioxide; hypromellose; pregelatinised maize starch; purified talc; iron oxide yellow; lactose monohydrate; maize starch; propylene glycol - zaldiar is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.