ARX-SUNITINIB sunitinib (as malate) 50 mg capsule blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

arx-sunitinib sunitinib (as malate) 50 mg capsule blister pack

arrotex pharmaceuticals pty ltd - sunitinib malate, quantity: 66.825 mg (equivalent: sunitinib, qty mg) - capsule, hard - excipient ingredients: gelatin; mannitol; magnesium stearate; titanium dioxide; purified water; croscarmellose sodium; povidone; iron oxide black; iron oxide yellow; iron oxide red; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - arx-sunitinib is indicated for:,? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

ARX-SUNITINIB sunitinib (as malate) 37.5 mg capsule blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

arx-sunitinib sunitinib (as malate) 37.5 mg capsule blister pack

arrotex pharmaceuticals pty ltd - sunitinib malate, quantity: 50.119 mg (equivalent: sunitinib, qty mg) - capsule, hard - excipient ingredients: gelatin; mannitol; magnesium stearate; titanium dioxide; purified water; croscarmellose sodium; povidone; iron oxide yellow; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - arx-sunitinib is indicated for:,? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).

APO-URSODEOXYCHOLIC ACID ursodeoxycholic acid 250 mg capsule blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

apo-ursodeoxycholic acid ursodeoxycholic acid 250 mg capsule blister pack

arrotex pharmaceuticals pty ltd - ursodeoxycholic acid, quantity: 250 mg - capsule - excipient ingredients: titanium dioxide; maize starch; silicon dioxide; gelatin; magnesium stearate - ursodeoxycholic acid is indicated in the treatment of chronic cholestatic liver diseases.

MOXOTENS moxonidine 200 microgram tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

moxotens moxonidine 200 microgram tablet blister pack

arrotex pharmaceuticals pty ltd - moxonidine, quantity: 200 microgram - tablet, film coated - excipient ingredients: povidone; lactose monohydrate; magnesium stearate; crospovidone; titanium dioxide; hypromellose; purified talc; macrogol 6000; iron oxide red - moxotens is indicated for the treatment of hypertension.

MOXOTENS moxonidine 400 microgram tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

moxotens moxonidine 400 microgram tablet blister pack

arrotex pharmaceuticals pty ltd - moxonidine, quantity: 400 microgram - tablet, film coated - excipient ingredients: crospovidone; magnesium stearate; lactose monohydrate; povidone; titanium dioxide; hypromellose; purified talc; macrogol 6000; iron oxide red - moxotens is indicated for the treatment of hypertension.

TAMSIL terbinafine (as hydrochloride) 250 mg tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

tamsil terbinafine (as hydrochloride) 250 mg tablet blister pack

arrotex pharmaceuticals pty ltd - terbinafine hydrochloride, quantity: 281.25 mg (equivalent: terbinafine, qty 250 mg) - tablet - excipient ingredients: hypromellose; colloidal anhydrous silica; croscarmellose sodium; microcrystalline cellulose; magnesium stearate - treatment in adults of ringworm (tinea corporis, tinea cruris and tinea pedis) due to infection caused by dermatophytes such as trichophyton (e.g. t. rubrum, t. mentagrophytes, t. verrucosum, t. violaceum), microsporum canis and epidermophyton floccosum, where oral therapy is considered appropriate owing to the site, severity or extent of the infection, and the infection is not responsive to topical therapy. onychomycosis in adults (fungal infection of the nail) caused by dermatophyte fungi.

AMITRIPTYLINE-ARX amitriptyline hydrochloride 50 mg tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

amitriptyline-arx amitriptyline hydrochloride 50 mg tablet blister pack

arrotex pharmaceuticals pty ltd - amitriptyline hydrochloride, quantity: 50 mg - tablet - excipient ingredients: lactose monohydrate; microcrystalline cellulose; maize starch; croscarmellose sodium; colloidal anhydrous silica; purified talc; magnesium stearate; macrogol 6000; hypromellose; titanium dioxide; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350 - for the treatment of major depression. entrip 50mg tablets are indicated only for the maintenance treatment of major depression (see precautions). nocturnal enuresis where organic pathology has been excluded.

AMITRIPTYLINE-ARX amitriptyline hydrochloride 25 mg tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

amitriptyline-arx amitriptyline hydrochloride 25 mg tablet blister pack

arrotex pharmaceuticals pty ltd - amitriptyline hydrochloride, quantity: 25 mg - tablet - excipient ingredients: lactose monohydrate; microcrystalline cellulose; maize starch; croscarmellose sodium; colloidal anhydrous silica; purified talc; magnesium stearate; macrogol 6000; hypromellose; titanium dioxide; iron oxide yellow; polyvinyl alcohol; macrogol 3350 - for the treatment of major depression. nocturnal enuresis where organic pathology has been excluded.

AMITRIPTYLINE-ARX amitriptyline hydrochloride10 mg tablet blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

amitriptyline-arx amitriptyline hydrochloride10 mg tablet blister pack

arrotex pharmaceuticals pty ltd - amitriptyline hydrochloride, quantity: 10 mg - tablet - excipient ingredients: lactose monohydrate; microcrystalline cellulose; maize starch; croscarmellose sodium; colloidal anhydrous silica; purified talc; magnesium stearate; macrogol 6000; hypromellose; titanium dioxide; brilliant blue fcf aluminium lake; polyvinyl alcohol; macrogol 3350 - for the treatment of major depression. nocturnal enuresis where organic pathology has been excluded.

ARX-SUNITINIB sunitinib (as malate) 25 mg capsule blister pack Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

arx-sunitinib sunitinib (as malate) 25 mg capsule blister pack

arrotex pharmaceuticals pty ltd - sunitinib malate, quantity: 33.413 mg (equivalent: sunitinib, qty 25 mg) - capsule, hard - excipient ingredients: gelatin; mannitol; magnesium stearate; iron oxide red; titanium dioxide; purified water; croscarmellose sodium; povidone; iron oxide yellow; iron oxide black; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - arx-sunitinib is indicated for:,? treatment of advanced renal cell carcinoma (rcc),? treatment of gastrointestinal stromal tumour (gist) after failure of imatinib mesilate treatment due to resistance or intolerance,? treatment of unresectable, well-differentiated pancreatic neuroendocrine tumours (pancreatic net).