Alkali metal amide and imide systems especially NaNH 2 and Li 2 NH have recently been proposed as a catalyst for NH 3 cracking. This finding ignites the interest of researchers worldwide to study amide−imide/amide−hydride systems. Although these systems have shown catalytic properties toward NH 3 cracking and have also been proposed as a hydrogen storage material, the decomposition mechanism of sodium amide is still unclear due to the complexity and low melting point of NaNH 2 . Herein, pure NaNH 2 and its composite with lithium hydride as well as sodium hydride in a molar ratio 1:1 has been investigated, and a detailed mechanism associated with their decomposition has been suggested. The sodium amide−lithium hydride system is found to be analogous to lithium amide−sodium hydride. It desorbs 4 wt % H 2 through cation exchange in a temperature range of 25−200 °C followed by NH 3 mediated reaction in the temperature range 200−400 °C. The desorbed product can be rehydrogenated at around 200 °C under 2.0 MPa. An important intermediate, a double cation amide, i.e., Li 3 Na(NH 2 ) 4 , is formed during the decomposition process. The mechanism for the formation of this double cation amide and successive H 2 desorption is proposed herein. The two-peak mystery in the analogous LiNH 2 −NaH system remained unknown for almost a decade and is cracked herein during this study. We successfully propose our model based on NH 3 mediated reaction for the decomposition of sodium amide−alkali hydride composite system.