Pays: Australie
Langue: anglais
Source: Department of Health (Therapeutic Goods Administration)
diclofenac sodium, Quantity: 25 mg
Novartis Pharmaceuticals Australia Pty Ltd
Tablet, enteric coated
Excipient Ingredients: purified talc; povidone; iron oxide yellow; maize starch; PEG-40 hydrogenated castor oil; lactose monohydrate; magnesium stearate; colloidal anhydrous silica; hypromellose; microcrystalline cellulose; acrylates copolymer; macrogol 8000; titanium dioxide; sodium starch glycollate; steareth-2; simethicone; sorbic acid
Oral
20, 50
Medicine Registered
(S4) Prescription Only Medicine
INDICATIONS AS AT 19 MAY 2004: Inflammatory and degenerative forms of rheumatism: rheumatoid arthritis and osteoarthritis. Relief of acute or chronic pain states in which there is an inflammatory component. Symptomatic treatment of primary dysmenorrhoea.
Visual Identification: yellow, round, slightly biconvex tablets with bevelled edges. Imprinted with BZ on one side and CG on the other; Container Type: Bottle; Container Life Time: 4 Years; Container Temperature: Store below 30 degrees Celsius
Registered
1991-08-02