The developmental toxicity potential of ametryn was assessed, involving teratogenic and reproductive studies on 180 and 170 presumed pregnant albino mice respectively, given doses of 0, 292, 438, 584 and 779 mg kg -1 day -1 , orally on days 6-15 of presumed gestation. During the gestation period, body weight, food consumption, water intake, mortality and general behavioural changes were recorded. On day 18, mice for teratogenic studies were killed and some parameters assessed. There were more deaths for the 584 mg kg -1 day -1 (31%) and 779 mg kg -1 day -1 (49%) groups than for the 438 mg kg -1 day -1 (10%) and 292 mg kg -1 day -1 (0%) groups. Reductions in mean body weight gain during exposure and post-exposure periods were recorded for the two highest dose levels; however, the corrected maternal weight (minus the uterus) remained unchanged for all the groups. Differences in food consumption and water intake were insignificant at all dose levels. Teratogenic parameters such as litter size decreased at the two highest doses as a result of significant resorptions and abortions. Other parameters such as termed fetuses per litter, fetal body weight, placental weight, crown-rump length and tail length, were reduced significantly. No external, visceral or skeletal changes were observed except delayed ossification. These results show that ametryn is embryotoxic to mice at 584 mg kg -1 and above. The 170 presumed pregnant mice (F 0 ) allowed to deliver F 1 pups did so after 20(±2) days and F 2 pups obtained from matured F 1 (not given any ametryn) were also delivered after 20(±1) days. There was F 1 pup weight reduction for the two highest doses whereas F 2 pups showed a non-significant reduction only for 779 mg kg -1 day -1 group. F 1 fetal viability was 50-75% before day 4 and 75-99% after day 4 for the two highest doses compared to 100% survival for other dosage groups. No deaths were recorded for F 2 generation pups. Food and water intakes, crown-rump length and tail length increments were insignificant for both generations. The appearance of developmental milestones like pinna attachment, hair growth, vaginal opening and testes descension remained unaffected for all the doses, but times of incisor eruptions, eye and ear opening were slightly lengthened for F 1 generation at 779 mg kg -1 . This observation was not noted in F 2 generation pups. A battery of behavioural tests conducted for F 1 and F 2 pups did not reveal changes in movements such as pivoting, negative geotaxis reflex nor in post-weaning test such as consummatory activity and activity wheel. The growth of the skeletal system was unaffected by ametryn after day 10 post-delivery (F 1 generation) and day 0 (F 2 ) generation. Ametryn has little or no effect on reproductive and/or developmental characteristics of mice at doses below maternal toxicity.