Time-resolved Fourier transform infrared emission spectroscopy is used to measure the nascent rovibrational distribution of low-lying electronically excited NH2((A) over tilde (2)A(1)) produced in the 193.3 nm photolysis of room-temperature and jet-cooled ammonia. Emission is observed predominantly from NH2((A) over tilde) states with rotational motion about the a-axis and without bending excitation, upsilon(2)'=0. A bimodal N-'=K-a' rotational state population distribution is observed with up to K-a'=7 in upsilon(2)'=0 and with maxima at K-a'=5 and K-a'=1. We suggest that the bimodal rotational distribution may result from the competition between planar and bent geometries during dissociation. Weaker emission from NH2((A) over tilde) with bending excitation, upsilon(2)'=1 and 2, is detected; the upsilon(2)'=1, N'=K-a' rotational state population distribution spans from K-a'=0 to the energetic limit of K-a'=4. The vibrational energy partitioning for the formation of NH2((A) over tilde,upsilon(2)'=0):NH2((A) over tilde,upsilon(2)'=1) is 3:1 and 2:1 in the room-temperature and jet-cooled conditions, respectively. An upper limit of the NH2((A) over tilde,upsilon(2)'=2) population is similar to 10% of the total NH2((A) over tilde) photofragments. Emission from rotational states with N'> K-a' (molecules with rotational excitation about the b/c-axes) is also observed. Under jet-cooled conditions the NH2(A) b/c-axes rotational temperature of similar to 120 K is higher than that expected from the rotationally cold parent species and is attributed to a mapping of the zero-point bending motion in the nu(4) H-N-H scissors bending coordinate of the NH3((A) over tilde) predissociative state onto the NH2((A) over tilde,upsilon(2)',N',K-a')+H photofragments.