In a developmental toxicity study (MRID number if available) [Chemical name (% a.i.)] was administered to [(# of females) strain, species]/dose in [diet, water, by capsule, by gavage] at dose levels of 0, x, x, or x   mg/kg bw/day from days [#] through [#] of gestation.

[Describe maternal toxicity briefly.  If none, state that there were no treatment-related effects in mortality, clinical signs, body weight, food consumption, or cesarean parameters]. The maternal LOAEL is       mg/kg bw/day, based on [endpoint].  The maternal NOAEL is       mg/kg bw/day.  Describe effects at doses > LOAEL.

[Describe developmental toxicity briefly.  If none, state that there were no treatment-related effects in developmental parameters]. The developmental LOAEL is       mg/kg bw/day, based on [endpoint].  The developmental NOAEL is      mg/kg bw/day. Describe effects at doses > LOAEL.

The developmental toxicity study in the rabbit is classified [acceptable, unacceptable(why); note if it is a range-finding study] and satisfies (does not satisfy) the guideline requirement for a developmental toxicity study (OPPTS 870.3700; OECD 414) in [species].  [If it does not satisfy the requirement, concisely list only major deficiencies or refer to deficiency section.]