Bioequivalence Study of Metformin 1000 mg Tablets Immediate Release (IR) Versus Glucophage® 1000 mg Tablets IR In Healthy Subjects

Inclusion Criteria: * Signed informed consent form. * Healthy male and female subjects aged 18 to 45 years. * Verified diagnosis is "healthy" according to data Standard clinical, laboratory and Instrumental methods of examination. * Have a body mass index between 18,5 and 27 kg/m2. * Females must have a negative pregnancy test. * Subjects must use, with their partner, methods of highly effective contraception throughout the study and 30 days after the end of study. Exclusion Criteria: * History of serious allergic problems/events * Medicinal intolerance. * History of allergic reactions to memantine or investigator's product components * Any acute and chronic diseases of the cardiovascular system, cardiovascular, bronchopulmonary, neuroendocrine systems, as well as diseases of the gastrointestinal tract, liver, kidneys, blood. * Acute infectious diseases in less than 4 weeks before the start of the study. * Subjects who have taken medication 4 weeks preceding before the study. * Subjects who have taken any drugs known effects on hemodynamics or to induce or inhibit hepatic drug metabolism within 30 days prior to administration of the study medication (examples of inducers: barbiturates, omeprazole, etc.). * Donation of plasma (450 mL or more) within 2 month prior to administration of the study medication. * History of significant alcohol or drugs abuse or any indication of the regular use of more than 10 units of alcohol per week (1 Unit = 200 mL of wine or 500 mL of beer o…