Present approach demonstrates a speedy and competent in vitro regeneration method for A. lebbeck. The hypocotyl explants (HP) excised from a 15-day-old seedlings were cultured on Murashige and Skoog (MS) medium supplemented with different concentrations (0.5, 2.5, 5.0, 7.5, 10.0 and 12.5 lM) of 6-Benzyladenine (BA), Kinetin (Kn) and 2-Isopentenyl adenine (2-iP) singly as well as in combination with a-naphthalene acetic acid (NAA) or Indole-3-butyric acid (IBA) or Indole-3-acetic acid (IAA; 0.1, 0.5, 1.0, 1.5 and 2.0 lM). The best shoot regeneration rate (88 %) with number of shoots (34.00 ± 1.15) and shoot length (6.30 ± 0.05 cm) per explant was obtained on MS ? BA (7.5 lM) ? NAA (0.5 lM) after 8 weeks of culture. While, the explants cultured onto the MS ? TDZ (Thidiazuron; 0.5, 1.0, 2.5, 5.0 and 7.5 lM) singly showed maximum shoot proliferation response of 77 % when, TDZ exposed cultures were transferred on the BA (7.5 lM) ? NAA (0.5 lM) supplied MS medium producing maximum no. of shoots (20.30 ± 0.32) and shoot length (5.15 ± 0.08 cm) after 8 weeks of culture. The regenerated