RADPHARM DIDA powder for injection Australia - English - Department of Health (Therapeutic Goods Administration)

radpharm dida powder for injection

global medical solutions australia pty limited t/a radpharm scientific - etifenin, quantity: 20 mg; stannous chloride, quantity: 0.42 mg - injection, powder for - excipient ingredients: - indications as at 25 september 1996: technetium (99mtc) etifenin may be used as a hepatobiliary imaging pharmaceutical.

Ifenin 200 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ifenin 200 mg film-coat. tabl.

aurobindo pharma b.v. - ibuprofen 200 mg - film-coated tablet - 200 mg - ibuprofen 200 mg - ibuprofen

Ifenin 400 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ifenin 400 mg film-coat. tabl.

aurobindo pharma b.v. - ibuprofen 400 mg - film-coated tablet - 400 mg - ibuprofen 400 mg - ibuprofen

BACTIFENIN Tablet Kenya - English - Pharmacy and Poisons Board

bactifenin tablet

tablets (india) limited. no 72 marshalls road chennai 600008 - co-trimoxazole tablets - tablet - trimethoprim bp 80 mg sulphamethoxazole bp 400 mg - antibacterials for systemic use: combinations of

Bactifenin Oral Suspension Kenya - English - Pharmacy and Poisons Board

bactifenin oral suspension

til healthcare ltd no 72 marshalls road chennai 600008 - co-trimoxazole oral suspension - oral suspension - trimethoprim bp 40 mg, sulphamethoxazole bp 200… - antibacterials for systemic use: combinations of

FERROSIG INJECTION iron 100mg/2mL (as polymaltose) injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

ferrosig injection iron 100mg/2ml (as polymaltose) injection ampoule

sigma company limited - iron polymaltose, quantity: 318 mg (equivalent: iron, qty 100 mg) - injection, solution - excipient ingredients: sodium hydroxide; water for injections; hydrochloric acid - indications as at 8 april 2002: for the treatment of iron deficiency anaemia in the following circumstances: * when oral therapy is contraindicated. * when enteric absorption of iron is defective. * when patient non-compliance or persistent gastrointestinal intolerance makes oral therapy impractical.

OFEV nintedanib (as esilate) 150 mg soft capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

ofev nintedanib (as esilate) 150 mg soft capsule blister pack

boehringer ingelheim pty ltd - nintedanib esilate, quantity: 180.6 mg (equivalent: nintedanib, qty 150 mg) - capsule, soft - excipient ingredients: iron oxide red; titanium dioxide; hard fat; lecithin; gelatin; glycerol; iron oxide yellow; medium chain triglycerides; propylene glycol; butan-1-ol; isopropyl alcohol; strong ammonia solution; iron oxide black; ethanol; shellac; sulfuric acid - ofev is indicated in combination with docetaxel for the treatment of patients with locally advanced, metastatic or recurrent non-small cell lung cancer (nsclc) of adenocarcinoma tumour histology after failure of first line chemotherapy.,ofev is indicated for the treatment of idiopathic pulmonary fibrosis (ipf).,ofev is also indicated for the treatment of other chronic fibrosing interstitial lung diseases (ilds) with a progressive phenotype.,ofev is indicated for slowing the rate of decline in pulmonary function in patients with systemic sclerosis-associated interstitial lung disease (ssc-ild).