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Trials / Completed

CompletedNCT00913718

To Demonstrate the Relative Bioavailability of Geneva and Dista (Prozac) 20 mg Fluoxetine Hydrochloride Capsules (Pulvules) In Healthy Adult Males Under Fasting Conditions

Comparative, Randomized, Single-Dose, 2-way Crossover Bioavailability Study of Geneva and Dista (Prozac) 20 mg Fluoxetine Hydrochloride Capsules (Pulvules) In Health Adult Males Under Fasting Conditions Following Administration of a 40 mg Dose

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Sandoz · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

To demonstrate the relative bioavailability of Geneva and Dista (Prozac) 20 mg Fluoxetine Hydrochloride capsules (Pulvules) in healthy adult males under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGFluoxetine Hydrochloride 20 mg Capsules (Geneva Pharmaceutical, Inc.)
DRUGProzac Fluoxetine Hydrochloride 20 mg Capsules (Dista)

Timeline

Start date
1996-06-01
Primary completion
1996-07-01
Completion
1996-07-01
First posted
2009-06-04
Last updated
2017-03-28

Source: ClinicalTrials.gov record NCT00913718. Inclusion in this directory is not an endorsement.

To Demonstrate the Relative Bioavailability of Geneva and Dista (Prozac) 20 mg Fluoxetine Hydrochloride Capsules (Pulvul (NCT00913718) · Clinical Trials Directory