Objective:To study the leaf epidermis of wild and micropropagated Dioscorea bulbifera Linn.(D.bulbifera)in order to document useful diagnostic features that may be employed for correct crude drug identification and to clear any taxonomic uncertainties in the micropropagated medicinal plant.Methods:Growth responses of micropropagated D.bulbifera were observed on Murashige Skoog medium supplemented with 6-benzylamino purine(1.0 mg/L)+α-naphthaleneacetic acid(0.2 mg/L)+cysteine(20 mg/L)using nodal segments as explants.Leaves of the wild and micropropagated plants were studied microscopically.Results:More than 80%shoot regeneration and formation of 10%-30%whitish-brown callus were observed within 3 weeks.The highest root proliferation was obtained from Murashige Skoog medium of 6-benzylamino purine(0.05 mg/L)andα-naphthaleneacetic acid(0.01 mg/L)with mean root length of(27.00±1.25)mm and elongated single shoot of mean length(38.00±11.09)mm.Leaf epidermal features that revealed similarities between the wild and micropropagated plants included amphistomatic condition,presence of mucilage,glandular unicellular trichome with multicellular head,polygonal cells with smooth walls,stomata type and shape.Slight variations included thick cuticular wall with closed stomata in wild plant compared to thin walled opened stomata in the in vitro plant.Opening of stomata accounted for larger average stomata sizes of(7.68±0.38)μm and(6.14±0.46)μm on the adaxial and abaxial surfaces,respectively of the micropropagated plant compared to the wild.Conclusions:The diagnostic features obtained in the study could serve as a basis for proper identification for quality control for standardization of the medicinal plant. Objective: To study the leaf epidermis of wild and micropropagated Dioscorea bulbifera Linn. (D. bulbifera) in order to document useful diagnostic features that may be employed for correct crude drug identification and to clear any taxonomic uncertainties in the micropropagated medicinal plant. Methods: Growth responses of micropropagated D. bulbifera were observed on Murashige Skoog medium supplemented with 6-benzylamino purine (1.0 mg / L) + α-naphthaleneacetic acid (0.2 mg / L) + cysteine ​​(20 mg / L) using nodal segments as explants. Leaves of the wild and micropropagated plants were studied microscopically. Results: More than 80% shoot regeneration and formation of 10% -30% whitish-brown callus were observed within 3 weeks. The highest root proliferation was obtained from Murashige Skoog medium of 6- The mean root length of (27.00 ± 1.25) mm and elongated single shoot of mean length (38.00 ± 11.09) mm. Leaf epidermal features that revealed similari (0.05 mg / L) and α-naphthaleneacetic acid ties between the wild and micropropagated plants included amphistomatic conditions, presence of mucilage, glandular unicellular trichome with multicellular head, polygonal cells with smooth walls, stomata type and shape. light variations included thick cuticular wall with closed stomata in wild plant compared to thin walled opened stomata in the in vitro plant. Opening of stomata accounts for larger average stomata sizes of (7.68 ± 0.38) μm and (6.14 ± 0.46) μm on the adaxial and abaxial surfaces, respectively of the micropropagated plant compared to the wild. Conclusions: The diagnostic features obtained in the study could serve as a basis for proper identification for quality control for standardization of the medicinal plant.