European Union - English - EMA (European Medicines Agency)

sandoz gmbh - pregabalin - anxiety disorders; epilepsy - antiepileptics, - epilepsypregabalin sandoz gmbh is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.generalised anxiety disorderpregabalin sandoz gmbh is indicated for the treatment of generalised anxiety disorder (gad) in adults.

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

fresenius kabi australia pty ltd - calcium chloride dihydrate, quantity: 67.5 mg; sodium chloride, quantity: 1.5 g; sodium lactate, quantity: 792.5 mg; potassium chloride, quantity: 100 mg - injection, solution - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - compound sodium lactate (hartmann's solution) is used:,? for intravenous fluid and electrolyte replacement,? as a source of bicarbonate in the treatment of mild to moderate metabolic acidosis associated with dehydration or associated with potassium deficiency,? as a vehicle for intravenous drug delivery, if the drugs are compatible with the solutions.

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

fresenius kabi australia pty ltd - sodium lactate, quantity: 3.17 g/l; sodium chloride, quantity: 6 g/l; potassium chloride, quantity: 0.4 g/l; calcium chloride dihydrate, quantity: 0.27 g/l - injection, intravenous infusion - excipient ingredients: water for injections - compound sodium lactate (hartmann's solution) injection is used for intrvenous fluid and electrolyte replacement, as a source of bicarbonate in the treatment of mild to moderate metabolic acidosis associated with dehydration or associated with potassium deficiency, and as a vehicle for intravenous drug delivery, if the drugs are compatible with the solutions.

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

fresenius kabi australia pty ltd - sodium lactate, quantity: 3.17 g/l; sodium chloride, quantity: 6 g/l; potassium chloride, quantity: 0.4 g/l; calcium chloride dihydrate, quantity: 0.27 g/l - injection, intravenous infusion - excipient ingredients: water for injections - compound sodium lactate (hartmann's solution) injection is used for intrvenous fluid and electrolyte replacement, as a source of bicarbonate in the treatment of mild to moderate metabolic acidosis associated with dehydration or associated with potassium deficiency, and as a vehicle for intravenous drug delivery, if the drugs are compatible with the solutions.

Zimbabwe - English - Medicines Control Authority

aculife healthcare private ltd - compound sodium lactate - injectable; iv (infusion) - 3.2; 6; 0.4; 0.27g

Kenya - English - Pharmacy and Poisons Board

aculife healthcare pvt ltd commerce house-v, besides vodafone house, prahlad - compound sodium lactate intravenous infusion b.p… - infusion - each 100 ml contains sodium lactate 0.320 gm… - intravenous solutions: solutions affecting the

Uganda - English - National Drug Authority

aculife healthcare pvt ltd - compound sodium lactate - parenteral ordinary infusion vials/bottles - multi ingredient

New Zealand - English - Medsafe (Medicines Safety Authority)

psm healthcare ltd trading as api consumer brands - compound cardamom tincture - oral solution - 100% - active: compound cardamom tincture

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

henry schein halas - 38764 - light-cured dental restorative composite resin - composite restorative and filling material for core build-ups and root post cementation thereby helping restore damaged dental tissues. the shade involved try match the colour of the original teeth for aesthetic reasons.

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

life healthcare pty ltd - 46585 - prosthesis, knee, internal, insert component - composed of uhmw-pe. the symmetric acs fb pe-inserts are fixed to the tibial component via a snap-fit mechanism. the fb pe-insert ultra features a highly congruent articulation between femoral component and pe-insert. thereby an increased stability is provided in flexion and extension. a pe insert component of the acs knee system. the acs knee system is indicated, if - severe joint destruction with significant impairment where other therapeutic measures are not more promising. - severe joint pain due to degenerative or rheumatoid arthritis, joint fractures or bone necrosis. - post-operative conditions after previous surgery with or without the use of implants.