minitran 15 glyceryl trinitrate 15mg/24 hour transdermal drug delivery system, sachet
inova pharmaceuticals (australia) pty ltd - glyceryl trinitrate, quantity: 54 mg - drug delivery system, transdermal - excipient ingredients: ethyl oleate; glyceryl laurate; acrylates/acrylamide copolymer - prevention of chronic stable angina pectoris due to coronary artery disease.
minitran 10 glyceryl trinitrate 10mg/24 hour transdermal drug delivery system, sachet
inova pharmaceuticals (australia) pty ltd - glyceryl trinitrate, quantity: 36 mg - drug delivery system, transdermal - excipient ingredients: ethyl oleate; glyceryl laurate; acrylates/acrylamide copolymer - prevention of chronic stable angina pectoris due to coronary artery disease.
minitran 5 glyceryl trinitrate 5mg/24hour transdermal drug delivery system, sachet
inova pharmaceuticals (australia) pty ltd - glyceryl trinitrate, quantity: 18 mg - drug delivery system, transdermal - excipient ingredients: ethyl oleate; glyceryl laurate; acrylates/acrylamide copolymer - prevention of chronic stable angina pectoris due to coronary artery disease.
vocabria cabotegravir (as sodium) 30 mg film-coated tablet, bottle
viiv healthcare pty ltd - cabotegravir, quantity: 30 mg (equivalent: cabotegravir sodium, qty mg) - tablet, film coated - excipient ingredients: titanium dioxide; magnesium stearate; hypromellose; lactose monohydrate; microcrystalline cellulose; sodium starch glycollate type a; macrogol 3350 - vocabria tablets are indicated in combination with rilpivirine tablets for the short-term treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults who are virologically suppressed (hiv-1 rna <50 copies/ml) and have no known or suspected resistance to either cabotegravir or rilpivirine (see sections 4.2 dose and method of administration and 5.1 pharmacodynamic properties, clinical trials) for: ? oral lead in to assess tolerability of cabotegravir prior to administration of cabotegravir prolonged-release suspension for injection plus rilpivirine prolonged-release suspension for injection. ? oral therapy for adults who will miss planned dosing with cabotegravir prolonged-release suspension for injection.
ivaswift 5 (ivabradine tablets 5mg)
synerrv sdn bhd - ivabradine oxalate -
ivaswift 7.5 (ivabradine tablets 7.5mg)
synerrv sdn bhd - ivabradine oxalate -
abraxane
bristol-myers squibb pharma eeig - paclitaxel - breast neoplasms; pancreatic neoplasms; carcinoma, non-small-cell lung - antineoplastic agents - abraxane monotherapy is indicated for the treatment of metastatic breast cancer in adult patients who have failed first-line treatment for metastatic disease and for whom standard, anthracycline containing therapy is not indicated.abraxane in combination with gemcitabine is indicated for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas.abraxane in combination with carboplatin is indicated for the first-line treatment of non-small cell lung cancer in adult patients who are not candidates for potentially curative surgery and/or radiation therapy.
abraxane
neopharm scientific ltd - paclitaxel - powder for suspension for infusion - paclitaxel 100 mg/vial - paclitaxel - abraxane monotherapy is indicated for the treatment of metastatic breast cancer in adult patients who have failed first-line treatment for metastatic disease and for whom standard, anthracycline containing therapy is not indicated. abraxane in combination with gemcitabine is indicated for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas. abraxane in combination with carboplatin is indicated for the first-line treatment of non-small cell lung cancer in adult patients who are not candidates for potentially curative surgery and/or radiation therapy.
vocabria
viiv healthcare b.v. - cabotegavir sodium, cabotegravir - hiv infections - antivirals for systemic use - vocabria tablets are indicated in combination with rilpivirine tablets for the short-term treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults who are virologically suppressed (hiv-1 rna
tabrecta 150 mg
novartis israel ltd - capmatinib as dihydrochloride monohydrate - film coated tablets - capmatinib as dihydrochloride monohydrate 150 mg - capmatinib - tabrecta is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumors have a mutation that leads to mesenchymal-epithelial transition (met) exon 14 skipping as detected by an approved test.