Overview

Bioequivalence Study of Two Formulations of 10 mg Lisinopril Tablet Under Fasting Condition

Status:
Completed
Trial end date:
2013-02-01
Target enrollment:
Participant gender:
Summary
The present study was conducted to find out whether the bioavailability of 10 mg lisinopril tablets produced by PT Dexa Medica was equivalent to the tablets produced by the innovator (ZestrilĀ® 10 mg, PT Boehringer Ingelheim Indonesia, Indonesia, under license from Astra Zeneca UK Ltd.)
Phase:
N/A
Details
Lead Sponsor:
Dexa Medica Group
Treatments:
Angiotensin-Converting Enzyme Inhibitors
Lisinopril