CPC A61K 9/0019 (2013.01) [A61K 31/221 (2013.01); A61K 31/225 (2013.01); A61K 47/10 (2013.01); A61K 47/12 (2013.01); A61K 47/183 (2013.01)] | 1 Claim |
1. A pharmaceutical composition consisting of:
(i) therapeutically effective amount of succinylcholine chloride at a concentration of from about 5 mg/mL to 60 mg/mL;
(ii) propylene glycol as a stabilizing agent at a concentration of from about 20 mg/mL to about 300 mg/mL;
(iii) water as a solvent,
(iv) optionally one or more pH adjusting agents; and
(v) optionally sodium chloride as a tonicity contributing agent at a concentration of from about 1 mg/mL to about 50 mg/mL,
wherein the composition is in the form of a ready to use aqueous solution suitable for parenteral administration, and
wherein the aqueous solution is stable at room temperature for at least 30 days.
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