TIXOL 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

tixol 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

alphapharm pty ltd - duloxetine hydrochloride, quantity: 33.65 mg - capsule, enteric - excipient ingredients: titanium dioxide; triethyl citrate; hypromellose phthalate; sucrose; indigo carmine; hypromellose; gelatin; purified talc; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; iron oxide yellow; shellac; strong ammonia solution; maize starch - duloxetine capsules are indicated for the treatment of major depressive disorder (mdd).,treatment of diabetic peripheral neuropathic pain (dpnp). treatment of generalised anxiety disorder (gad).

SUTENT sunitinib (as malate) 50 mg capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

sutent sunitinib (as malate) 50 mg capsule blister pack

pfizer australia pty ltd - sunitinib malate, quantity: 66.8 mg (equivalent: sunitinib, qty 50 mg) - capsule - excipient ingredients: sodium lauryl sulfate; titanium dioxide; croscarmellose sodium; shellac; povidone; magnesium stearate; sodium hydroxide; gelatin; iron oxide black; iron oxide red; propylene glycol; mannitol; iron oxide yellow - sutent 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).

SUTENT sunitinib (as malate) 25 mg capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

sutent sunitinib (as malate) 25 mg capsule blister pack

pfizer australia pty ltd - sunitinib malate, quantity: 33.4 mg (equivalent: sunitinib, qty 25 mg) - capsule - excipient ingredients: sodium hydroxide; titanium dioxide; mannitol; shellac; sodium lauryl sulfate; iron oxide red; propylene glycol; povidone; croscarmellose sodium; magnesium stearate; gelatin; iron oxide black; iron oxide yellow - sutent 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).

SUTENT sunitinib (as malate) 12.5 mg capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

sutent sunitinib (as malate) 12.5 mg capsule blister pack

pfizer australia pty ltd - sunitinib malate, quantity: 16.7 mg (equivalent: sunitinib, qty 12.5 mg) - capsule - excipient ingredients: sodium hydroxide; propylene glycol; shellac; sodium lauryl sulfate; iron oxide red; mannitol; magnesium stearate; titanium dioxide; povidone; gelatin; croscarmellose sodium - sutent 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).

FURATEC  dimethyl fumarate 240 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

furatec dimethyl fumarate 240 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 240 mg - capsule, enteric - excipient ingredients: magnesium stearate; methacrylic acid copolymer; triethyl citrate; silicified microcrystalline cellulose; purified talc; croscarmellose sodium; colloidal anhydrous silica; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

AKM DIMETHYL FUMARATE dimethyl fumarate 240 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

akm dimethyl fumarate dimethyl fumarate 240 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 240 mg - capsule, enteric - excipient ingredients: croscarmellose sodium; triethyl citrate; silicified microcrystalline cellulose; methacrylic acid copolymer; magnesium stearate; colloidal anhydrous silica; purified talc; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

AKM DIMETHYL FUMARATE dimethyl fumarate 120 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

akm dimethyl fumarate dimethyl fumarate 120 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 120 mg - capsule, enteric - excipient ingredients: silicified microcrystalline cellulose; triethyl citrate; croscarmellose sodium; magnesium stearate; purified talc; methacrylic acid copolymer; colloidal anhydrous silica; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

FURATEC dimethyl fumarate 120 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

furatec dimethyl fumarate 120 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 120 mg - capsule, enteric - excipient ingredients: magnesium stearate; methacrylic acid copolymer; silicified microcrystalline cellulose; purified talc; croscarmellose sodium; colloidal anhydrous silica; triethyl citrate; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

PHARMACOR DIMETHYL FUMARATE dimethyl fumarate 120 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor dimethyl fumarate dimethyl fumarate 120 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 120 mg - capsule, enteric - excipient ingredients: croscarmellose sodium; magnesium stearate; methacrylic acid copolymer; triethyl citrate; purified talc; silicified microcrystalline cellulose; colloidal anhydrous silica; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

PHARMACOR DIMETHYL FUMARATE dimethyl fumarate 240 mg delayed release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor dimethyl fumarate dimethyl fumarate 240 mg delayed release capsule blister pack

pharmacor pty ltd - dimethyl fumarate, quantity: 240 mg - capsule, enteric - excipient ingredients: methacrylic acid copolymer; purified talc; silicified microcrystalline cellulose; triethyl citrate; colloidal anhydrous silica; croscarmellose sodium; magnesium stearate; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; polysorbate 80; sodium lauryl sulfate - it is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.