Steroid dependency (SD) and frequent relapses (FR) are common with steroid-sensitive nephrotic syndrome (SSNS). We assessed the effectiveness of daily levamisole in 36 children with SSNS with FR and/or SD. Twenty patients (group 1) were given levamisole 2–3 mg/kg q.o.d. for 4–24 months. Sixteen (group 2) had relapses within 3 months: 5 received levamisole q.d. for 3–18 months, and 11 q.d. for 6 months and then q.o.d. for 4–18 months. Follow-up was 4–36 (mean 20.4 ± 9.2) months. After therapy, relapses (4.82 ± 3.15 vs. 2.01 ± 2.5 in group 1; 5.97 ± 3.38 vs. 1.34 ± 2.1 in group 2; p < 0.05) and prednisolone doses (0.57 ± 0.37 vs. 0.15 ± 0.33 mg/kg/day in group 1; 0.61 ± 0.42 vs. 0.19 ± 0.35 mg/kg/day in group 2; p < 0.05) decreased. Relapse frequency, prednisolone dose, response percentage, and survival curves for remission did not differ between groups. Group 1 had five episodes of leukopenia, and group 2 had four. White blood cell counts normalized after levamisole was discontinued. Serum blood urea nitrogen/creatinine and alanine aminotransferase/aspartate aminotransferase levels were normal. Levamisole is effective in maintaining remission in children with SSNS and FR and/or SD. Daily levamisole can be considered when responses to q.o.d. usage are unsatisfactory.