Pajjiż: Awstralja
Lingwa: Ingliż
Sors: Department of Health (Therapeutic Goods Administration)
sunitinib malate, Quantity: 66.825 mg (Equivalent: sunitinib, Qty 50 mg)
Sun Pharma ANZ Pty Ltd
Capsule, hard
Excipient Ingredients: Gelatin; mannitol; magnesium stearate; titanium dioxide; purified water; croscarmellose sodium; povidone; iron oxide yellow; iron oxide black; iron oxide red; propylene glycol; butan-1-ol; isopropyl alcohol; Shellac; ethanol absolute; ammonia; potassium hydroxide
Oral
28 capsules
(S4) Prescription Only Medicine
SUNITINIB SUN 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).
Visual Identification: Hard gelatin Size 1 capsule with opaque caramel cap and opaque caramel body, self-lock imprinted with white ink RM56 on the cap and body; Container Type: Bottle; Container Material: HDPE; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure
Registered
2021-02-22