United Kingdom - English - VMD (Veterinary Medicines Directorate)

ceva animal health ltd - enalapril maleate - tablet - cardio vascular ace inhibitor - dogs

United Kingdom - English - VMD (Veterinary Medicines Directorate)

ceva animal health ltd - enalapril maleate - tablet - cardio vascular ace inhibitor - dogs

United Kingdom - English - VMD (Veterinary Medicines Directorate)

ceva animal health ltd - enalapril maleate - tablet - cardio vascular ace inhibitor - dogs

United Kingdom - English - VMD (Veterinary Medicines Directorate)

ceva animal health ltd - enalapril maleate - tablet - cardio vascular ace inhibitor - dogs

Australia - English - Department of Health (Therapeutic Goods Administration)

viatris pty ltd - verapamil hydrochloride, quantity: 80 mg - tablet, film coated - excipient ingredients: calcium hydrogen phosphate dihydrate; microcrystalline cellulose; colloidal anhydrous silica; croscarmellose sodium; magnesium stearate; hypromellose; sodium lauryl sulfate; macrogol 6000; purified talc; titanium dioxide - isoptin tablets 80mg (immediate release) are indicated for: hypertension; angina of effort; angina at rest; vasospastic angina (including prinzmetal's variant angina); tachyarrhythmias including paroxysmal supra-ventricular tachycardia; atrial fibrillation with rapid ventricular response; atrial flutter with rapid ventricular response.

Australia - English - Department of Health (Therapeutic Goods Administration)

viatris pty ltd - verapamil hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: calcium hydrogen phosphate dihydrate; microcrystalline cellulose; colloidal anhydrous silica; croscarmellose sodium; magnesium stearate; hypromellose; sodium lauryl sulfate; macrogol 6000; purified talc; titanium dioxide - isoptin tablets 40mg (immediate release) are indicated for: hypertension; angina of effort; angina at rest; vasospastic angina (including prinzmetal's variant angina); tachyarrhythmias including paroxysmal supra-ventricular tachycardia; atrial fibrillation with rapid ventricular response; atrial flutter with rapid ventricular response.

Australia - English - Department of Health (Therapeutic Goods Administration)

viatris pty ltd - verapamil hydrochloride, quantity: 80 mg - tablet, film coated - excipient ingredients: calcium hydrogen phosphate dihydrate; microcrystalline cellulose; colloidal anhydrous silica; croscarmellose sodium; magnesium stearate; hypromellose; sodium lauryl sulfate; macrogol 6000; purified talc; titanium dioxide - isoptin tablets 80mg (immediate release) are indicated for: hypertension; angina of effort; angina at rest; vasospastic angina (including prinzmetal's variant angina); tachyarrhythmias including paroxysmal supra-ventricular tachycardia; atrial fibrillation with rapid ventricular response; atrial flutter with rapid ventricular response.

Australia - English - Department of Health (Therapeutic Goods Administration)

viatris pty ltd - verapamil hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: calcium hydrogen phosphate dihydrate; microcrystalline cellulose; colloidal anhydrous silica; croscarmellose sodium; magnesium stearate; hypromellose; sodium lauryl sulfate; macrogol 6000; purified talc; titanium dioxide - anpec tablets 40mg (immediate release) are indicated for: hypertension; angina of effort; angina at rest; vasospastic angina (including prinzmetal's variant angina); tachyarrhythmias including paroxysmal supra-ventricular tachycardia; atrial fibrillation with rapid ventricular response; atrial flutter with rapid ventricular response.

Australia - English - Department of Health (Therapeutic Goods Administration)

sandoz pty ltd - amoxicillin trihydrate, quantity: 1148 mg (equivalent: amoxicillin, qty 1000 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; povidone; magnesium stearate; sodium starch glycollate type a; hypromellose; titanium dioxide; purified talc - amoxycillin sandoz is indicated in the treatment of acute exacerbation of chronic bronchitis. notes: therapy should be guided by bacteriologic studies including sensitivity tests and by clinical response. amoxycillin alone or in combination with another antibiotic, may be used in an emergency where the causative agent has yet to be identified. amoxycillin sandoz 1000mg tablets have not been shown to be bioequivalent to the 500mg and 250mg capsule formulations given in equivalent doses. therefore, amoxycillin sandoz 1000mg tablets and other forms of amoxycillin are not considered interchangeable. infections caused by pathogens with established penicllin g susceptibility should preferentially be treated with penicillin g.

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - lamivudine, quantity: 300 mg; abacavir sulfate, quantity: 702.76 mg (equivalent: abacavir, qty 600 mg) - tablet, film coated - excipient ingredients: hypromellose; titanium dioxide; sunset yellow fcf aluminium lake; macrogol 8000; croscarmellose sodium; magnesium stearate; colloidal anhydrous silica; microcrystalline cellulose - abacavir and lamivudine combination tablets are a combination of two nucleoside analogues (abacavir and lamivudine). ,abacavir and lamivudine combination tablets are indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection in adults and adolescents from 12 years of age.