Țară: Australia
Limbă: engleză
Sursă: Department of Health (Therapeutic Goods Administration)
cefaclor monohydrate, Quantity: 393.36 mg (Equivalent: cefaclor, Qty 375 mg)
Sun Pharma ANZ Pty Ltd
cefaclor monohydrate
Tablet, modified release
Excipient Ingredients: lactose monohydrate; colloidal anhydrous silica; purified talc; hyprolose; hypromellose; magnesium stearate; propylene glycol; purified water; isopropyl alcohol; iron oxide black; titanium dioxide; macrogol 400; indigo carmine aluminium lake
Oral
10 tablets
(S4) Prescription Only Medicine
For the treatment of the following infections caused by susceptible organisms, in adults and children 12 years and older: Lower respiratory infections, including community acquired pneumonia of mild to moderate severity (excluding atypical pneumonia), acute bronchitis and exacerbation of chronic bronchitis. Upper respiratory infections, including pharyngitis, tonsillitis and acute bacterial sinusitis. Symptomatic lower urinary tract infections, including cystitis. Skin and skin structure infections.
Visual Identification: Capsule shaped, biconvex, unscored, blue film-coated tablet, imprinted with "Cefaclor CD 375mg" in black.; Container Type: Blister Pack; Container Material: PVC/PVDC/Al; Container Life Time: 18 Months; Container Temperature: Store below 25 degrees Celsius
Registered
2011-08-09