SODIUM CHLORIDE- sodium chloride injection United States - English - NLM (National Library of Medicine)

sodium chloride- sodium chloride injection

fresenius kabi usa, llc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular, or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.

SODIUM CHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

sodium chloride injection, solution

hospira, inc. - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - intravenous solutions containing sodium chloride are indicated for parenteral replenishment of fluid and sodium chloride as required by the clinical condition of the patient. none known. to open tear outer wrap at notch and remove solution container. if supplemental medication is desired, follow directions below before preparing for administration. some opacity of the plastic due to moisture absorption during the sterilization process may be observed. this is normal and does not affect the solution quality or safety. the opacity will diminish gradually. to add medication preparation for administration (use aseptic technique) warning: do not use flexible container in series connections.

SODIUM CHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

sodium chloride injection, solution

icu medical inc. - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - intravenous solutions containing sodium chloride are indicated for parenteral replenishment of fluid and sodium chloride as required by the clinical condition of the patient. none known. to open tear outer wrap at notch and remove solution container. if supplemental medication is desired, follow directions below before preparing for administration. some opacity of the plastic due to moisture absorption during the sterilization process may be observed. this is normal and does not affect the solution quality or safety. the opacity will diminish gradually. to add medication preparation for administration (use aseptic technique) warning: do not use flexible container in series connections.

Sodium Chloride New Zealand - English - Medsafe (Medicines Safety Authority)

sodium chloride

baxter healthcare ltd - sodium chloride 20% - solution for injection - 20 % - active: sodium chloride 20% excipient: water for injection

Sodium Chloride BP 20% New Zealand - English - Medsafe (Medicines Safety Authority)

sodium chloride bp 20%

astrazeneca limited - sodium chloride 20%{relative} - solution for injection - 20% w/v - active: sodium chloride 20%{relative} excipient: hydrochloric acid water for injection

MONTELUKAST SODIUM tablet
MONTELUKAST SODIUM tablet, chewable United States - English - NLM (National Library of Medicine)

montelukast sodium tablet montelukast sodium tablet, chewable

hikma pharmaceuticals usa inc. - montelukast sodium (unii: u1o3j18sfl) (montelukast - unii:mhm278sd3e) - montelukast 10 mg - montelukast sodium tablets and montelukast sodium chewable tablets are indicated for the prophylaxis and chronic treatment of asthma in adults and pediatric patients 2 years of age and older. montelukast sodium tablets and montelukast sodium chewable tablets are indicated for prevention of exercise-induced bronchoconstriction (eib) in patients 6 years of age and older. montelukast sodium tablets and montelukast sodium chewable tablets are indicated for the relief of symptoms of seasonal allergic rhinitis in patients 2 years of age and older and perennial allergic rhinitis in patients 2 years of age and older. because the benefits of montelukast sodium may not outweigh the risk of neuropsychiatric symptoms in patients with allergic rhinitis [see warnings and precautions ( 5.1)] , reserve use for patients who have an inadequate response or intolerance to alternative therapies. montelukast sodium tablets and montelukast sodium chewable tablets are not indicated for the treatment of an acute asthma attack. ris

COLPREP KIT- sodium sulfate, potassium sulfate, and magnesium sulfate for oral solution powder, for solution United States - English - NLM (National Library of Medicine)

colprep kit- sodium sulfate, potassium sulfate, and magnesium sulfate for oral solution powder, for solution

kvk-tech, inc. - sodium sulfate (unii: 0ypr65r21j) (sodium sulfate anhydrous - unii:36kcs0r750), potassium sulfate (unii: 1k573lc5tv) (sulfate ion - unii:7is9n8kpmg), magnesium sulfate (unii: de08037sab) (magnesium cation - unii:t6v3lhy838) - sodium sulfate 17.5 g in 22.7 g - colprep kit is indicated for cleansing of the colon as a preparation for colonoscopy in adults. - gastrointestinal obstruction - bowel perforation - gastric retention - ileus - toxic colitis or toxic megacolon - known allergies to components of the kit [see description (11)] teratogenic effects: pregnancy category c. animal reproduction studies have not been conducted with colprep kit. it is also not known whether colprep kit can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. colprep kit should be given to a pregnant woman only if clearly needed. it is not known whether this drug is excreted in human milk. because many drugs are excreted in human milk, caution should be exercised when colprep kit is administered to a nursing woman. the safety and effectiveness of colprep kit have not been established in pediatric patients. of the 375 patients who received another oral formulation of sodium sulfate (17.5 g), potassium sulfate (3.13 g), and magnesium sulfate (1.6 g)

PHYSIOSOL- sodium chloride, sodium acetate anhydrous, sodium gluconate, potassium chloride, and magnesium chloride irrigant United States - English - NLM (National Library of Medicine)

physiosol- sodium chloride, sodium acetate anhydrous, sodium gluconate, potassium chloride, and magnesium chloride irrigant

hospira, inc. - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698), sodium acetate anhydrous (unii: nvg71zz7p0) (sodium cation - unii:lyr4m0nh37), sodium gluconate (unii: r6q3791s76) (sodium cation - unii:lyr4m0nh37), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152, chloride ion - unii:q32zn48698), magnesium chloride (unii: 02f3473h9o) (magnesium cation - unii:t6v3lhy838, chloride ion - unii:q32zn48698) - sodium chloride 526 mg in 100 ml - physiosol™ is indicated for all general irrigation, washing and rinsing purposes which permit use of a sterile, nonpyrogenic electrolyte solution. not for injection by usual parenteral routes. an electrolyte solution should not be used for irrigation during electrosurgical procedures.

SODUM ACETATE- sodium acetate injection, solution, concentrate United States - English - NLM (National Library of Medicine)

sodum acetate- sodium acetate injection, solution, concentrate

american regent, inc. - sodium acetate anhydrous (unii: nvg71zz7p0) (acetate ion - unii:569dqm74sc, sodium cation - unii:lyr4m0nh37) - sodium acetate anhydrous 328 mg in 1 ml - sodium acetate for injection, usp concentrate is indicated as a source of sodium in patients with restricted or no oral intake. it is also useful as an additive for preparing specific intravenous fluid formulas, when the needs of the patient cannot be met by standard electrolyte or nutrient solutions. sodium acetate for injection, usp concentrate is contraindicated in patients with hypernatremia.

SODIUM CHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

sodium chloride injection, solution

general injectables & vaccines, inc - sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698) - sodium chloride 9 mg in 1 ml - this parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.