A Study to Evaluate the Effects of Renal Function on Pharmacokinetics and Safety of DA-8010

Inclusion Criteria: \[Healthy Volunteer\] * Adult male or female, 19 years to 75 years * eGFR ≥ 90 mL/min/1.73m\^2 * Body weight over 45.0 kg and body mass index in the range of 18.0 to 40.0 kg/m\^2 * The subjects signed and dated informed consent form after hearing a detailed explanation of the study, fully understanding and determined voluntarily to participate * The subjects who are judged appropriate to participate this clinical trial according to the physical examination, laboratory examination and questionnaire \[Renal Impairment Patient\] * Adult male of female, 19 years to 75 years * eGFR \< 90 mL/min/1.73m\^2, not on dialysis * Body weight over 45.0 kg and body mass index in the range of 18.0 to 40.0kg/m\^2 * The subjects signed and dated informed consent form after hearing a detailed explanation of the study, fully understanding and determined voluntarily to participate * The subjects who are judged appropriate to participate this clinical trial according to the physical examination, laboratory examination and questionnaire Exclusion Criteria: * The subjects with acute illness * The subjects with a history of gastrointestinal disease or surgery that may affect the absorption of Investigational Product * The subjects hypersensitive to any of the Investigational Product components or other drug components * The subjects who have continuously consumed excessive smoking or alcohol within 6 months of screening, or who cannot stop smoking, caffeine, or alcohol intake during hospitalization * The subjects who have history of drug abuse * The subjects who are pregnant or lactating * The subjects who do not agree to exclude the possibility of pregnancy using the contraception from the date of the first administration of the Investigational Product until the 4 weeks after the last administration