Dopram v injectable msds sheets

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* IN CASE OF EMERGENCY: CHEMTREC 24 Hr. EmergencyTelephone 1.800.424.9300 The Hazardous Chemical Master List includes the Hazardous Ingredient(s) for each product, manufacturer, and contact info. An example is shown on this first page only. If a product is Non-Hazardous, it is listed and noted as such to indicate that is has been addressed. Doxapram is a white to off-white, odorless, crystalline powder that is stable in light and air. It is soluble in water, sparingly soluble in alcohol and practically insoluble in ether. Injectable products have a pH from 3.5-5. Benzyl alcohol or chlorobutanol is added as a preservative agent in the commercially available injections. Uses

* IN CASE OF EMERGENCY: CHEMTREC 24 Hr. EmergencyTelephone 1.800.424.9300 The Hazardous Chemical Master List includes the Hazardous Ingredient(s) for each product, manufacturer, and contact info. An example is shown on this first page only. If a product is Non-Hazardous, it is listed and noted as such to indicate that is has been addressed.

hospital, medical office) for its sole intended parenteral (injection) purpose. Otherwise, use appropriate engineering control such as process enclosures, local exhaust ventilation, or other engineering controls including use of a biosafety cabinet / fume hood to control airborne levels below recommended exposure limits. Zoetis Inc. believes that the information contained in this Safety Data Sheet is accurate, and while it is provided in good faith, it is without warranty of any kind, expressed or implied. If data for a hazard are not included in this document there is no known information at this time. End of Safety Data Sheet DOPRAM Injection (doxapram hydrochloride injection, USP) NOT FOR USE IN NEONATES CONTAINS BENZYL ALCOHOL R x only DESCRIPTION DOPRAM Injection (doxapram hydrochloride injection, USP) is a clear, colorless, sterile, non-pyrogenic, aqueous solution with pH 3.5 to 5, for intravenous administration. Each 1 mL contains: BY I.V. INJECTION (See Table I. Dosage for postanesthetic use-—I.V.) The recommended dose for I.V. administration is 0.5 to 1 mg/kg for a single injection and at 5-minute intervals. Careful observation of the patient during administration and for some time subsequently are advisable. The maximum total dosage by I.V. injection is 2 mg/kg.