Terbinafine HCl 250 mg Tablet Formulations Under Non-Fasting Conditions

Exclusion Criteria

• •If female, pregnant, lactating or likely to become pregnant during the study.
• •History of allergy or sensitivity to terbinafine, or history of any drug hypersensitivity or intolerance which, in the opinion of the Investigator, would compromise the safety of the subject or the study.
• •Significant history or current evidence of chronic evidence of chronic infectious disease, system disorder ot organ dysfunction.
• •Presence of gastrointestinal disease ot history of malabsorption within the last year.
• •History of psychiatric disorders occuring within the last two years that required hospitalization or medication.
• •Presence of a medical condition requiring regular treatment with prescription drugs.
• •Use of pharmacologic agents known to significantly induce or inhibit drug-metabolizing enzymes. within 30 days prior to dosing.
• •Receipt of any drug as part of a research study within 30 days prior to dosing.
• •Drug or alcohol addition requiring treatment in the past 12 months.
• •Donation or significant loss of whole blood (480 ml or more) within 30 days or plasma within 14 days prior to dosing.
• •Positive test results for drug of abuse at screening.
• •Tobacco user within 90 days of the first study dose.
• •Unable, or unwilling to tolerate multiple venipunctures.