Journal of Bioequivalence & Bioavailability

Damodar R, Movva B, Mallikarjun PN, Pasumarthy C, Kona N, Varsha PV (2014) Formulation and evaluation of fast dissolving tablets of diclofenac sodium by novel hole technology. J Mol Pharm Org Process Res 2:2-6.

Parthasarathi D, Gajendra C, Dattatreya A, Sree Venkatesh Y (2011) Analysis of pharmacokinetic & pharmacodynamic models in oral and transdermal dosage forms. J Bioequiv Availab 3:268-276.

Vlase L, Kiss B, Muntean D, LeucuÅ£a SE (2010) Rapid high-performance liquid chromatography–tandem mass spectrometry method for determination of pentoxifylline and its active metabolites M1 and M5 in human plasma and its application in bioavailability study. Talanta 82:945-951.

Ravali R, Phaneendra M, Bhanu JK, Ramya SL, Sushma K (2011) Recent trends in analytical techniques for the development of pharmaceutical drugs. J Bioanal Biomed S 11:1-7.

Nishant T, Sathish Kumar D, Arun Kumar PM (2011) Role of pharmacokinetic studies in drug discovery. J Bioequiv Availab 3:263-267.

Cavalcanti AL, Reis MY, Silva GC, Ramalho ÍM, Guimarães GP, Silva JA, et al. (2016) Microemulsion for topical application of pentoxifylline: in vitro release and in vivo evaluation. Int J Pharm 506:351-360.

Farooq U, Malviya R, Kumar Sharma P (2014) Investigation and Need of Bioequivalence Study: Methodology and Regulatory Requirement. Appl Clin Res Clin Trials Regul Affairs 1:93-106.

Moreno I, Ochoa D, Román M, Cabaleiro T, Abad‐Santos F (2016) Effect of Truncating AUC at 12, 24 and 48 hr When Evaluating the Bioequivalence of Drugs with a Long Half‐Life. Basic Clin Pharmacol Toxicol 118:53-57.

Varsha YM. Ram Mohan Rao G, Venkateswara Rao V (2011) Cutting Edge Approach on Prodrug: Contrivance for Target Drug Delivery. J Bioequiv Availab 3:286-290.

Lees P, Hunter RP, Reeves PT, Toutain PL (2012) Pharmacokinetics and pharmacodynamics of stereoisomeric drugs with particular reference to bioequivalence determination. J Vet Pharmacol Ther 35:17-29.

Khandave SS, Onkar SV, Sawant SV, Joshi SS (2010) Evaluation of Performance of the Truncated Area Under Curve (AUC) as a Primary Pharmacokinetic Parameter in Bioequivalence Studies. J Bioequiv Availab 2:77-80.

Ravali R, Phaneendra M, Bhanu JK, Ramya SL, Sushma K (2011) Recent trends in analytical techniques for the development of pharmaceutical drugs. J Bioanal Biomed S 11:1-7.

Nishant T, Sathish Kumar D, Arun Kumar PM (2011) Role of pharmacokinetic studies in drug discovery. J Bioequiv Availab 3:263-267.

Damodar R, Movva B (2014) Preparation and.

Beerepoot PC (2017) Pharmacological Chaperones of the Dopamine Transporter: A Strategy for Increasing Function of Wild Type and Mutant Transporter (Doctoral dissertation).

Jain R, Praveen R, Iyer SS, Kumar S, Khuroo AH (1983) Development, Validation and Successful Application of an In vitro-In vivo Correlation. Psychiatry 44:82-84.

Jain R, Radhakrishnan P, S Iyer S, Kumar S, H Khuroo A (2017) Development, Validation and Successful Application of an In Vitro-In Vivo Correlation Model for Sustained Release Tablets of Bupropion Hydrochloride. Curr Bioactive Compounds 13:326-332.

Mansoursadeghi-Gilan T (2015) Real-world Effectiveness of Bupropion versus Varenicline for Smoking Cessation: Exploring the Role of Metabolic and Personality Variables (Doctoral dissertation).

Cotreau MM, Massmanian L, Strahs AL, Slichenmyer W, Vargo DL (2014) The effect of food on the pharmacokinetics of tivozanib hydrochloride. Clin Pharm Drug Develop 3:158-162.

Abdulrahman SA, Basavaiah K (2011) Application of ion-association titration for the assay of bupropion hydrochloride in pharmaceuticals. Chemical Industry and Chemical Engineering Quarterly/CICEQ 17:299-306.