• Yadav Dinesh
• Harsh Chunara
• Dr. Hiral Panchal
• Dr.Mittal Maheshwari

Immediate release tablets of Gabapentin were successfully formulated by employing direct compression method. Preformulation studies of drug were performed; the infrared spectral analysis revealed that there is no chemical interaction with excipients used was compatible with drugs. Based on Weight variation, Hardness, friability, and Drug Content it was found that all the formulation were satisfied mention criteria as per Pharmacopoeial Standards. Disintegration time in F13 formulation found 17 sec and dispersion time found 15 sec. The in vitro drug release was 99 %. Overall, in the formulations prepared by direct compression method, F13 which contain 4 % CCS as Super disintegrants releases 99 % drug in 2 minutes was found the best formulation. Stability study of F13 batch was found stable for 1 month.

Gabapentin, Weight variation, Disintegration time ,Immediate release tablets.

"TITLE: FORMULATION DEVELOPMENT AND EVALUATION OF GABAPENTIN IMMEDIATE RELEASE TABLETS", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.8, Issue 5, page no.c418-c428, May-2021, Available :http://www.jetir.org/papers/JETIR2105309.pdf

"TITLE: FORMULATION DEVELOPMENT AND EVALUATION OF GABAPENTIN IMMEDIATE RELEASE TABLETS", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.8, Issue 5, page no. ppc418-c428, May-2021, Available at : http://www.jetir.org/papers/JETIR2105309.pdf