An implantable drug depot for reducing, preventing or treating pain and/or inflammation in a patient in need of such treatment, the implantable drug depot comprising sulindac or a pharmaceutically acceptable salt thereof in an amount of from about 20 wt. % to about 40 wt. % of the drug depot, and at least one polymer, wherein the at least one polymer comprises one or more of poly(lactide-co-glycolide), D-lactide, D,L-lactide, L-lactide, D,L-lactide-caprolactone, glycolide-caprolactone, or D,L-lactide-glycolide-caprolactone and said drug depot is capable of releasing the sulindac or pharmaceutically acceptable salt thereof over a period of at least 3 days.