The gas phase vibrational spectroscopy of the protonated ammonia dimer N(2)H(7)(+), a prototypical system for strong hydrogen bonding, is studied in the spectral region from 330 to 1650 cm(-1) by combining infrared multiple photon dissociation and multidimensional quantum mechanical simulations. The fundamental transition of the antisymmetric proton stretching vibration is observed at 374 cm(-1) and assigned on the basis of a six-dimensional model Hamiltonian, which predicts this transition at 471 cm(-1). Photodissociation spectra of the larger protonated ammonia clusters NH(4)(+)(NH(3))(n) with n=2-4 are also reported for the range from 1050 to 1575 cm(-1). The main absorption features can be assigned within the harmonic approximation, supporting earlier evidence that hydrogen bonding in these clusters is considerably weaker than for n=1.