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Vinpocetine is being used worldwide by people of all ages, including pregnant women, for its purported multiple health benefits. However, limited data is available addressing the safety/toxicity of vinpocetine. The National Toxicology Program conducted studies to examine potential effects of vinpocetine on the developing rat. Disposition data is helpful to put the fetal findings into context and provide information on the potential risk for humans.The current study reports the systemic exposure and toxicokinetic (TK) parameters of vinpocetine and metabolite, apovincaminic acid (AVA), in pregnant Harlan Sprague Dawley rats, fetuses and amniotic fluid following oral gavage exposure of dams to 5 and 20 mg/kg vinpocetine from gestational day 6 to 18. Vinpocetine was absorbed rapidly in dams with a maximum plasma concentration (Cmax) reaching ≤ 1.37 h. Predicted Cmax and area under the concentration versus time curve (AUC) increased less than proportionally to the dose. Vinpocetine was rapidly distributed to the peripheral compartment. More importantly, significant transfer of vinpocetine from dam to fetuses was observed with fetal Cmax and AUC ≥ 55% of dams. Vinpocetine was cleared rapidly from dam plasma with an elimination half-life of ≤ 4.02 h with no apparent dose-related effect. Vinpocetine was rapidly and highly metabolized to AVA with AVA plasma levels in dams ≥ 2.7-fold higher than vinpocetine, although in the fetuses, AVA levels were much lower than vinpocetine. Comparison of current rat data with literature human data demonstrates that systemic exposure to vinpocetine in rats following repeated exposure to 5 mg/kg is similar to that following a single human relevant dose of 10 mg suggesting that the findings from the toxicology study may be relevant to humans.The NTP is investigating the effect of vinpocetine on the developing rat.To put the fetal findings into context we investigated the systemic exposure.Vnpocetine was absorbed rapidly in dams with fetal Cmax and AUC ≥ 55% of dams.Systemic exposure in rats following 5 mg/kg is similar to human dose of 10 mg.This suggests findings from the toxicology study may be relevant to humans.