New Zealand - engelsk - Medsafe (Medicines Safety Authority)

carsl consulting - rifaximin 550mg;  ;  ;   - film coated tablet - 550 mg - active: rifaximin 550mg       excipient: colloidal silicon dioxide disodium edetate glyceryl diisostearate hypromellose iron oxide red microcrystalline cellulose propylene glycol purified talc purified water sodium starch glycolate titanium dioxide - prevention of the recurrence of hepatic encephalopathy where other treatments have failed or are contraindicated.

Storbritannia - engelsk - MHRA (Medicines & Healthcare Products Regulatory Agency)

norgine pharmaceuticals ltd - rifaximin - oral tablet - 550mg

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

atnahs pharma australia pty ltd - naproxen sodium, quantity: 550 mg - tablet, film coated - excipient ingredients: purified water; microcrystalline cellulose; povidone; magnesium stearate; purified talc; titanium dioxide; hypromellose; macrogol 8000; indigo carmine - crysanal is indicated as an analgesic in acute migraine attacks, for the treatment of gout, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis and for the relief of acute and/or chronic pain states in which there is an inflammatory component.

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

atnahs pharma australia pty ltd - naproxen sodium, quantity: 550 mg - tablet, film coated - excipient ingredients: magnesium stearate; povidone; purified water; purified talc; microcrystalline cellulose; titanium dioxide; hypromellose; macrogol 8000; indigo carmine - anaprox is indicated as an analgesic in acute migraine attacks, for the treatment of gout, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis and for the relief of acute and/or chronic pain states in which there is an inflammatory component.

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

atnahs pharma netherlands b.v. - naproxen sodium 550 mg - film-coated tablet - 550 mg - naproxen sodium 550 mg - naproxen

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

krka d.d. novo mesto d.d. - naproxen sodium 550 mg - eq. naproxen 500 mg - film-coated tablet - 550 mg - naproxen sodium 550 mg - naproxen

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

eg sa-nv - naproxen sodium 550 mg - film-coated tablet - 550 mg - naproxen sodium 550 mg - naproxen

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

norgine b.v. - rifaximin 550 mg - film-coated tablet - 550 mg - rifaximin 550 mg - rifaximin

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

alfasigma s.p.a. - rifaximin 550 mg - film-coated tablet - 550 mg - rifaximin 550 mg - rifaximin

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

stallergenes australia pty ltd - honey bee venom, quantity: 550 microgram - injection, powder for - excipient ingredients: mannitol; sodium chloride - indicated use of allergenic extracts is for the diagnosis and treatment (hypo-sensitization therapy) of patients who experience allergic symptoms.