A Study to Determine Bioequivalence of Isotretinoin in Healthy Male Subjects Under Fed Condition

Inclusion Criteria: * Included in study will be male volunteers. * Ages between 18 and 45 years old. * BMI (Body Mass Index) between 20 to 26 kilogram/meter square (kg/m\^2). * Anti-doping tests negative results. * Negative test results for Ac human immunodeficiency virus (HIV), HBsAg (hepatitis B surface antigen), and rapid plasma regain (RPR; syphilis test). * Clinical biochemical test values: Hematic Biometry, Urine Analysis, Biochemical Profile: (Glucose, Ureic Nitrogen, Urea, Creatinine, Uric Acid, Cholesterol, Triglycerides, Total Proteins, Albumin, Globulin, Bilirubin (total, indirect and direct), Alkaline Phosphatase (ALP), Lactic Dehydrogenase, Asparate aminotransferase (AST), Alanine aminotransferase (ALT), Calcium, Phosphorus, Sodium, Potassium, Chlorine and Iron), Ac HIV, HBsAg and RPR, must fall within an interval between minimum and maximum values in connection to said tests accepted values. * Normal Electrocardiogram (ECG) and Chest X-rays. * Complete the scale 'Columbia Suicide Severity Rating Scale' (C-SSRS), before and after each dosification period. * Obtain a grade of zero in the C-SSRS. * Signed the Informed Consent corresponding to the bioequivalence study. * In exception cases, accepted may be a candidate for which any previously mentioned test is exceeded regarding considered valid maximum and minimum accepted normal values, as long as it involves an isolated value and there are no other manifestations which could allow assuming that a given value is …