Abstract: This work was undertaken to investigate the individual effects and probable mechanism of action of chlorpromazine hydrochloride (largactil) and thioridazine hydrochloride (melleril) on male reproductive functions, in albino rats. A total of 45 adult male albino Wistar-strain rats were used. Five rats served as the control while the remaining forty rats were divided into four groups, of 10 rats each. Rats in group I were treated with 2.3 mg kg-1 BW, while those of group II received 5.7 mg kg-1 BW of chlorpromazine. Rats in group III, were treated with 1.7 mg kg-1 BW, while those of group IV received 2.3 mg kg-1 BW of thioridazine. Control rats received vehicle of the drugs (i.e. distilled water). Drugs and vehicle were administered orally on a daily basis. Five rats, in each of the four drug-treated groups served as the recovery rats. Sperm characteristics evaluation, serum levels of testosterone and histopathological alterations in the testis were assessed both after four weeks of continuous drug administrations and four weeks of drug withdrawal. Chlorpromazine and thioridazine significantly caused a reduction in the absolute weights of the testis, epididymis and seminal vesicles (p<0.01) at high and low doses. Weight of the prostate gland was also reduced significantly (p<0.05) at the high dose. The epididymal sperm motility, viability (life/death ratio) and counts were significantly reduced (p<0.01) at high dose of chlorpromazine and thioridazine. Moreover, sperm morphological abnormalities were significantly increased (p<0.01) at both doses of the drugs. Reduction in serum levels of testosterone for both drugs was statistically significant (p<0.01). The histopathological alterations observed in the testis includes moderate to severe degeneration of seminiferous tubular epithelium. Fertility and other associated changes were restored within four weeks of cessation of treatment. Chlorpromazine and thioridazine appear to have reversible antifertility actions in male albino rats. These actions were probably mediated within the testis and epididymis.