BAXTER 0.3% SODIUM CHLORIDE and 3.3% GLUCOSE 500mL injection AHB1033 Australija - engleski - Department of Health (Therapeutic Goods Administration)

baxter 0.3% sodium chloride and 3.3% glucose 500ml injection ahb1033

baxter healthcare pty ltd - glucose, quantity: 33 g/l; sodium chloride, quantity: 3 g/l - injection, solution - excipient ingredients: water for injections - sodium chloride (%) and glucose (%) intravenous infusion is indicated for replenishing fluid losses, as an energy source and for restoration or maintenance of sodium and chloride ion concentrations. it may be used as a vehicle of drug delivery where intravenous delivery is appropriate and the drug is compatible with this solution.

BAXTER 0.45% SODIUM CHLORIDE and 2.5% GLUCOSE 500mL injection AHB1023 Australija - engleski - Department of Health (Therapeutic Goods Administration)

baxter 0.45% sodium chloride and 2.5% glucose 500ml injection ahb1023

baxter healthcare pty ltd - glucose, quantity: 25 g/l; sodium chloride, quantity: 4.5 g/l - injection, solution - excipient ingredients: hydrochloric acid; water for injections - sodium chloride (%) and glucose (%) intravenous infusion is indicated for replenishing fluid losses, as an energy source and for restoration or maintenance of sodium and chloride ion concentrations. it may be used as a vehicle of drug delivery where intravenous delivery is appropriate and the drug is compatible with this solution.

MEMANTINE HYDROCHLORIDE capsule, extended release Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

memantine hydrochloride capsule, extended release

ani pharmaceuticals, inc. - memantine hydrochloride (unii: jy0wd0ua60) (memantine - unii:w8o17sjf3t) - memantine hydrochloride extended-release capsules are indicated for the treatment of moderate to severe dementia of the alzheimer's type. memantine hydrochloride extended-release capsules are contraindicated in patients with known hypersensitivity to memantine hydrochloride or to any excipients used in the formulation. risk summary there are no adequate data on the developmental risk associated with the use of memantine hydrochloride extended-release capsules in pregnant women. adverse developmental effects (decreased body weight and skeletal ossification) were observed in the offspring of rats administered memantine during pregnancy at doses associated with minimal maternal toxicity. these doses are higher than those used in humans at the maximum recommended daily dose of memantine hydrochloride extended-release capsules [see data]. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. the ba

Sodium Chloride BP 0.9% Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

sodium chloride bp 0.9%

astrazeneca limited - sodium chloride 0.9% - solution for injection - 0.9% w/v - active: sodium chloride 0.9% excipient: hydrochloric acid water for injection

Phebra SODIUM CHLORIDE 23.4% 2.34 g in 10 mL concentrated  injection for infusion vial Australija - engleski - Department of Health (Therapeutic Goods Administration)

phebra sodium chloride 23.4% 2.34 g in 10 ml concentrated injection for infusion vial

phebra pty ltd - sodium chloride, quantity: 234 mg/ml - injection, concentrated - excipient ingredients: water for injections; hydrochloric acid; sodium hydroxide - indications as at 01 january 1991 : as an additive to parenteral fluids in patients who have specific electrolyte needs for sodium or chloride ions. as a sclerosing agent for small symptomatic varicose veins.

SODIUM CHLORIDE injection Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

sodium chloride injection

nephron sc inc. - sodium chloride (unii: 451w47iq8x) (chloride ion - unii:q32zn48698) - sodium chloride injection, usp is indicated as a source of water and electrolytes. 0.9% sodium chloride injection, usp is also indicated for use as a priming solution in hemodialysis procedures. none known.

Potassium Chloride 20mmol in 0.9% Sodium Chloride (1000mL) Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

potassium chloride 20mmol in 0.9% sodium chloride (1000ml)

baxter healthcare ltd - potassium chloride 0.15%{relative}; sodium chloride 0.9%{relative} - solution for infusion - active: potassium chloride 0.15%{relative} sodium chloride 0.9%{relative} excipient: water for injection - indicated as a source of water and to restore electrolyte balance as required by the patient's clinical condition, such as hypokalaemia.

Potassium Chloride 30mmol in 0.9% Sodium Chloride (1000mL) Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

potassium chloride 30mmol in 0.9% sodium chloride (1000ml)

baxter healthcare ltd - potassium chloride 0.224%; sodium chloride 0.9% - solution for infusion - 30 mmol/l - active: potassium chloride 0.224% sodium chloride 0.9% - indicated as a source of water and to restore electrolyte balance as required by the patient's clinical condition, such as hypokalaemia.

Sodium Chloride 0.9% Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

sodium chloride 0.9%

multichem nz limited - sodium chloride 9 mg/ml - solution for injection - 0.9% w/v - active: sodium chloride 9 mg/ml excipient: water for injection

SODIUM CHLORIDE Irska - engleski - HPRA (Health Products Regulatory Authority)

sodium chloride

maco pharma (uk) ltd - sodium chloride - solution for infusion - 0.9 %w/v - electrolytes