Minneapolis, MN: Paddock Laboratories, Inc 2010.Ħ. Philadelphia, PA: Pharmaceutical Press 2012:1557.ĥ. Remington: The Science and Practice of Pharmacy. Washington, DC: American Pharmaceutical Association 2012:880-884.Ĥ. In: Rowe RC, Sheskey PJ, Cook WG, Fenton ME, eds. Standard operating procedure for performing physical quality assessment of oral and topical liquids. Sorbate and methylparaben as preservatives. Sodium phosphate, and citric acid as buffering agents, and potassium ItĬontains purified water, sucrose, glycerin, sorbitol (5%), flavoring, Ora-Sweet is buffered to a pH ofĪpproximately 4.2 and has an osmolality of about 3,240 mOsm/kg. It is flavored with a citrus-berry flavorīlend and contains glycerin and sorbitol to prevent “cap lock,” a
Ora-Sweet syrup vehicle is a flavoring vehicle for oralĮxtemporaneous preparations. Xanthan gum, carrageenan, sodium phosphate, and citric acid as bufferingĪgents, simethicone as an antifoaming agent, and potassium sorbate and Water, microcrystalline cellulose, sodium carboxymethylcellulose, Viscosity of approximately 1,000 cps at 25☌. Ora-Plus is an oral suspending vehicle that accepts dilution of up toĥ0% or more with water, flavoring agents, or syrups and still retains In polyvinylĬhloride IV solution bags, the agent has been reported to exhibit Methohexitone sodium, cefazolin, and phenytoin sodium. Incompatible in solution with amphotericin, sulfadiazine sodium, It is available in bothĪnhydrous and monohydrate forms. Melting point is in the range of 74☌ to 79☌. Lidocaine HCl should be protected from light, and its Has a pH in the range of 4.0 to 5.5, and the injection has a pH rangingįrom 5.0 to 7.0. Soluble in water (1:0.7) and in alcohol (1:1.5). Onset and an intermediate duration of action. It is an amide-type local anesthetic with a rapid MW 288.81) occurs as a white, odorless, crystalline powder with a Sodium carboxymethylcellulose to adjust viscosity, sodium hydroxide toĪdjust pH to 6.0 to 7.0, and purified water. Mg/mL, methylparaben, propylparaben, cherry essence, saccharin sodium, Xylocaine Viscous 2% contains lidocaine hydrochloride 20 Prolonged contact is possible, owing to this agent’s high It hasĪ low surface tension, which provides for an even film over the mucous
Xylocaine Viscous 2% (lidocaine hydrochloride) is a clear to almostĬlear, slightly colored, viscous liquid with an odor of cherries. It is miscible with most polar solventsĪnd is chemically stable in all physical states (ice, liquid, and Specific gravity of 0.9971 at room temperature, a melting point of 0☌,Īnd a boiling point of 100☌. Purified water is water that is obtained by distillation, ionĮxchange, reverse osmosis, or some other suitable process.
It isĪvailable as extended-release oral capsules and tablets, solution, Morphine sulfate is soluble in water,įreely soluble in hot water, and slightly soluble in alcohol. Morphine sulfate gradually loses water of hydration. Masses of crystals, or a white, crystalline powder. Is odorless and occurs as white, feathery, silky crystals, cubical Treatment of severe, acute pain or moderate-to-severe chronic pain. MW 758.83) is a phenanthrene-derivative opiate agonist used in the Irritated or inflamed mucous membranes of the mouth and pharynx Relief of moderate-to-severe pain and discomfort in connection with Stability (discoloration, foreign materials, gas formation, moldĭiscussion: This preparation has been used for Rheologic properties/pourability, physical observation, and physical Weight/volume, pH, specific gravity, active drug assay, color, Quality Control: Quality-control assessment can include Stability: A beyond-use date of up to 14 days when stored in a refrigerator may be used for this preparation. Packaging: Package in tight, light-resistant containers. Use: This preparation has been used in the treatment of oral pain. Add 40 mL of Ora-Plus,įollowed by sufficient Ora-Sweet to final volume, and mix well. Dissolve the morphine sulfate in the purified Method of Preparation : Calculate the quantity ofĮach ingredient for the amount to be prepared.
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