Country: Ástralía
Tungumál: enska
Heimild: Department of Health (Therapeutic Goods Administration)
exemestane, Quantity: 25 mg
Arrotex Pharmaceuticals Pty Ltd
Exemestane
Tablet, film coated
Excipient Ingredients: colloidal anhydrous silica; sodium starch glycollate type A; hypromellose; mannitol; microcrystalline cellulose; magnesium stearate; crospovidone; polysorbate 80; titanium dioxide; macrogol 400
Oral
90 Tablets, 30 Tablets, 15 Tablets
(S4) Prescription Only Medicine
Exemestane is indicated for the sequential adjuvant treatment of oestrogen receptor-positive early breast cancer in post-menopausal women who have received prior adjuvant tamoxifen therapy. . Exemestane is indicated for the treatment of oestrogen receptor-positive advanced breast cancer in women with natural or induced postmenopausal status whose disease has progressed following anti-oestrogen therapy.
Visual Identification: White to off-white, round, biconvex film-coated tablets debossed with 'E25' on one side and plain on the other.; Container Type: Blister Pack; Container Material: PVC/PVDC/Al; Container Life Time: 30 Months; Container Temperature: Store below 25 degrees Celsius
Licence status A
2017-02-09