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. 2017 Sep 19;103(3):502–510. doi: 10.1002/cpt.760

Table 2.

Summary data of bioequivalence (BE) analysis, via standard BE population ratio method, following noncompartmental pharmacokinetic analysis of Isoniazid and Rifampin in Native (N) and Co‐encapsulated (CoE) formulations of Rifamate using tools within FDA‐recognized Phoenix WinNonlin software (Certera)

Isoniazid Rifampin
Cmax AUC Cmax AUC
Bioequivalence confidence level 95.00 95.00 95.00 95.00
Ratio N/CoE 94.547746 97.194316 82.072826 90.668841
Ratio test Bioequivalence shown Bioequivalence shown Bioequivalence shown Bioequivalence shown