Land: Australië
Taal: Engels
Bron: Department of Health (Therapeutic Goods Administration)
propranolol hydrochloride, Quantity: 40 mg
Ipca Pharma (Australia) Pty Ltd
Propranolol hydrochloride
Tablet
Excipient Ingredients: lactose monohydrate; maize starch; quinoline yellow; brilliant blue FCF aluminium lake; sunset yellow FCF aluminium lake; magnesium stearate; povidone; sodium starch glycollate
Oral
100
(S4) Prescription Only Medicine
Angina pectoris; Hypertension; Prevention of migraine; Cardiac dysrhythmias: certain intrinsic cardiac dysrhythmias; dysrhythmias associated with thyrotoxicosis; anxiety tachycardia; certain drug-induced dysrhythmias (eg tachycardia due to digitalis or adrenaline overdosage); Essential tremor, including familial and senile tremor; Phaeochromocytoma (only with concurrent alpha-receptor blockade); Hypertrophic subaortic stenosis; Suspected or definite myocardial infarction; Fallot?s tetralogy
Visual Identification: Green coloured, round, biconvex tablets, embossed with "P" and "40" on either side of the breakline on one side and plain on the other side.; Container Type: Bottle; Container Material: HDPE; Container Life Time: 36 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure
Licence status A
2015-02-13