| CPC A61K 31/4985 (2013.01) [A61K 9/16 (2013.01); A61K 31/505 (2013.01); A61P 31/00 (2018.01); A61P 31/18 (2018.01)] | 30 Claims |
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1. A parenteral pharmaceutical suspension comprising 0.1-50% by weight a compound of formula (I)
![]() or a pharmaceutically acceptable salt thereof,
0.1-10% by weight polysorbate,
0.1-10% by weight polyethylene glycol 3350, 4000 or 8000,
mannitol, and
water,
wherein the suspension has mean particle size of 0.1-1 μm, and
wherein the suspension has been sterilized by gamma irradiation.
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