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

accord healthcare pty ltd - glimepiride, quantity: 4 mg - tablet, uncoated - excipient ingredients: magnesium stearate; lactose monohydrate; sodium starch glycollate type a; povidone - glimepiride apotex is indicated as an adjunct to diet, exercise and weight loss to lower the blood glucose in patients with non-insulin-dependent diabetes mellitus (type 2)

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

accord healthcare pty ltd - glimepiride, quantity: 3 mg - tablet, uncoated - excipient ingredients: magnesium stearate; povidone; lactose monohydrate; iron oxide yellow; sodium starch glycollate type a - glimepiride apotex is indicated as an adjunct to diet, exercise and weight loss to lower the blood glucose in patients with non-insulin-dependent diabetes mellitus (type 2)

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

accord healthcare pty ltd - glimepiride, quantity: 2 mg - tablet, uncoated - excipient ingredients: povidone; lactose monohydrate; magnesium stearate; sodium starch glycollate type a; iron oxide red - glimepiride apotex is indicated as an adjunct to diet, exercise and weight loss to lower the blood glucose in patients with non-insulin-dependent diabetes mellitus (type 2)

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

accord healthcare pty ltd - glimepiride, quantity: 1 mg - tablet, uncoated - excipient ingredients: povidone; magnesium stearate; sodium starch glycollate type a; lactose monohydrate; iron oxide red - glimepiride apotex is indicated as an adjunct to diet, exercise and weight loss to lower the blood glucose in patients with non-insulin-dependent diabetes mellitus (type 2)

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

arrotex pharmaceuticals pty ltd - lercanidipine hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: lactose monohydrate; sodium starch glycollate; iron oxide red; iron oxide yellow; polyvinyl alcohol; titanium dioxide; macrogol 3350; purified talc; magnesium stearate; microcrystalline cellulose; povidone - treatment of hypertension.

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

arrotex pharmaceuticals pty ltd - lercanidipine hydrochloride, quantity: 10 mg - tablet, film coated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; iron oxide yellow; polyvinyl alcohol; purified talc; macrogol 3350; titanium dioxide; magnesium stearate; sodium starch glycollate; povidone - treatment of hypertension.

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

southern cross pharma pty ltd - morphine sulfate pentahydrate, quantity: 100 mg - tablet, modified release - excipient ingredients: hyetellose; hypromellose; magnesium stearate; povidone; purified talc; titanium dioxide; iron oxide black; macrogol 400 - for the management of severe pain where other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. is not indicated for use in chronic non-cancer pain other than in exceptional circumstances. is not indicated as an as-needed (prn) analgesia.

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

southern cross pharma pty ltd - morphine sulfate pentahydrate, quantity: 60 mg - tablet, modified release - excipient ingredients: lactose monohydrate; magnesium stearate; hypromellose; povidone; hyetellose; purified talc; titanium dioxide; sunset yellow fcf aluminium lake; macrogol 400 - for the management of severe pain where other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. is not indicated for use in chronic non-cancer pain other than in exceptional circumstances. is not indicated as an as-needed (prn) analgesia.

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

southern cross pharma pty ltd - morphine sulfate pentahydrate, quantity: 30 mg - tablet, modified release - excipient ingredients: purified talc; hyetellose; lactose monohydrate; hypromellose; povidone; magnesium stearate; titanium dioxide; indigo carmine; sunset yellow fcf; erythrosine; macrogol 400 - for the management of severe pain where other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. is not indicated for use in chronic non-cancer pain other than in exceptional circumstances. is not indicated as an as-needed (prn) analgesia.

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

southern cross pharma pty ltd - morphine sulfate pentahydrate, quantity: 10 mg - tablet, modified release - excipient ingredients: povidone; hypromellose; magnesium stearate; hyetellose; purified talc; lactose monohydrate; titanium dioxide; iron oxide yellow; iron oxide red; macrogol 400 - for the management of severe pain where other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. is not indicated for use in chronic non-cancer pain other than in exceptional circumstances. is not indicated as an as-needed (prn) analgesia.