Parenteral metolazone formulations

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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A61K 3147

Patent

active

060488743

ABSTRACT:
The invention provides a method of making a pharmaceutical composition comprising a solution, which method comprises: (a) providing a solvent comprising propylene glycol, polyethylene glycol, polypropylene glycol, or glycerin; and (b) adding metolazone. The final concentration of metolazone in the solution is 9 mg/ml or more, the metolazone is not precipitated, and the concentration of metolazone is above its apparent equilibrium solubility. The invention also provides a pharmaceutical composition comprising a solution comprising: (a) a solvent other than water; and (b) 9 mg/ml or more of metolazone. The metolazone is not precipitated in this solution and the concentration of metolazone is above its apparent equilibrium solubility.

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Belair, "the Renal Pharmacology of Metolazone, 2-Methyl-3-0-Tolyl-6-Sulfamyl-7-Chloro-1,2,3, 4-Tetrahydro-4-Quinazolinone," Research Communications in Chemical Pathology and Pharmacology, vol. 2, No. 1, pp. 98-117 (1971).
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