Sunitinib Pfizer New Zealand - English - Medsafe (Medicines Safety Authority)

sunitinib pfizer

pfizer new zealand limited - sunitinib malate 50.1mg equivalent to sunitinib 37.5mg;   - capsule - 37.5 mg - active: sunitinib malate 50.1mg equivalent to sunitinib 37.5mg   excipient: croscarmellose sodium gelatin ink iron oxide yellow magnesium stearate mannitol povidone sodium laurilsulfate titanium dioxide - treatment of advanced renal cell carcinoma

Sutent New Zealand - English - Medsafe (Medicines Safety Authority)

sutent

pfizer new zealand limited - sunitinib malate 50.1mg equivalent to 37.5mg sunitinib;   - capsule - 37.5 mg - active: sunitinib malate 50.1mg equivalent to 37.5mg sunitinib   excipient: croscarmellose sodium gelatin ink iron oxide yellow magnesium stearate mannitol povidone sodium laurilsulfate titanium dioxide - sutent is indicated for the treatment of advanced renal cell carcinoma.

Sunitinib Dr.Reddy's New Zealand - English - Medsafe (Medicines Safety Authority)

sunitinib dr.reddy's

dr reddy's new zealand limited - sunitinib malate 50.1mg equivalent to sunitinib 37.5 mg - capsule - 37.5 mg - active: sunitinib malate 50.1mg equivalent to sunitinib 37.5 mg excipient: croscarmellose sodium gelatin iron oxide yellow magnesium stearate mannitol povidone sodium laurilsulfate titanium dioxide water - treatment of advanced renal cell carcinoma 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) 37.5 mg  capsul blister pack. Australia - English - Department of Health (Therapeutic Goods Administration)

sutent sunitinib (as malate) 37.5 mg capsul blister pack.

pfizer australia pty ltd - sunitinib malate, quantity: 50.1 mg (equivalent: sunitinib, qty 37.5 mg) - capsule - excipient ingredients: propylene glycol; iron oxide black; isopropyl alcohol; butan-1-ol; ammonia; ethanol absolute; titanium dioxide; povidone; purified water; potassium hydroxide; mannitol; shellac; croscarmellose sodium; iron oxide yellow; magnesium stearate; sodium lauryl sulfate; gelatin - 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) 37.5 mg capsule bottle Australia - English - Department of Health (Therapeutic Goods Administration)

sutent sunitinib (as malate) 37.5 mg capsule bottle

pfizer australia pty ltd - sunitinib malate, quantity: 50.1 mg (equivalent: sunitinib, qty 37.5 mg) - capsule - excipient ingredients: sodium lauryl sulfate; ethanol absolute; ammonia; butan-1-ol; iron oxide yellow; croscarmellose sodium; potassium hydroxide; mannitol; povidone; shellac; purified water; iron oxide black; titanium dioxide; propylene glycol; isopropyl alcohol; magnesium stearate; gelatin - 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).

SUNITINIB MALATE capsule United States - English - NLM (National Library of Medicine)

sunitinib malate capsule

mylan pharmaceuticals inc. - sunitinib malate (unii: lvx8n1ut73) (sunitinib - unii:v99t50803m) - sunitinib malate capsules are indicated for the treatment of adult patients with gastrointestinal stromal tumor (gist) after disease progression on or intolerance to imatinib mesylate. sunitinib malate capsules are indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc). sunitinib malate capsules are indicated for the adjuvant treatment of adult patients at high risk of recurrent rcc following nephrectomy. sunitinib malate capsules are indicated for the treatment of progressive, well-differentiated pancreatic neuroendocrine tumors (pnet) in adult patients with unresectable locally advanced or metastatic disease. none. based on animal reproduction studies and its mechanism of action, sunitinib can cause fetal harm when administered to a pregnant woman [see clinical pharmacology (12.1)] . there are no available data in pregnant women to inform a drug-associated risk. in animal developmental and reproductive toxicology studies, oral administration of sunitinib to pregnant rats and

Sunitinib Pfizer New Zealand - English - Medsafe (Medicines Safety Authority)

sunitinib pfizer

pfizer new zealand limited - sunitinib malate 16.7mg equivalent to sunitinib 12.5mg;   - capsule - 12.5 mg - active: sunitinib malate 16.7mg equivalent to sunitinib 12.5mg   excipient: croscarmellose sodium gelatin ink iron oxide red magnesium stearate mannitol povidone sodium laurilsulfate titanium dioxide - treatment of advanced renal cell carcinoma

Sunitinib Pfizer New Zealand - English - Medsafe (Medicines Safety Authority)

sunitinib pfizer

pfizer new zealand limited - sunitinib malate 33.4mg equivalent to sunitinib 25mg;   - capsule - 25 mg - active: sunitinib malate 33.4mg equivalent to sunitinib 25mg   excipient: croscarmellose sodium gelatin ink iron oxide black iron oxide red iron oxide yellow magnesium stearate mannitol povidone sodium laurilsulfate titanium dioxide - treatment of advanced renal cell carcinoma

Sutent Capsule 37.5mg Singapore - English - HSA (Health Sciences Authority)

sutent capsule 37.5mg

pfizer private limited - sunitinib malate 50.100mg eqv sunitinib - capsule - 37.5mg - sunitinib malate 50.100mg eqv sunitinib 37.5mg

SUNITINIB MSN sunitinib (as malate) 37.5 mg hard capsule bottle Australia - English - Department of Health (Therapeutic Goods Administration)

sunitinib msn sunitinib (as malate) 37.5 mg hard capsule bottle

accelagen pty ltd - sunitinib malate, quantity: 50.118 mg (equivalent: sunitinib, qty 37.5 mg) - capsule, hard - excipient ingredients: croscarmellose sodium; mannitol; gelatin; pregelatinised maize starch; titanium dioxide; magnesium stearate; iron oxide yellow; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - sunitinib msn 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)