A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting Conditions
Public ClinicalTrials.gov record NCT00865943. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Relative Bioavailability of 10 mg Citalopram Hydrobromide Tablets Under Fasting Conditions
Study identification
- NCT ID
- NCT00865943
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1
- Lead sponsor
- Actavis Inc.
- Industry
- Enrollment
- 26 participants
Conditions and interventions
Conditions
Interventions
- CELEXATM 10 mg tablets, single dose Drug
- Citalopram HBr eq. 10 mg tablets, single dose Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jun 30, 2003
- Primary completion
- Jul 31, 2003
- Completion
- Jul 31, 2003
- Last update posted
- Aug 16, 2010
2003
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| PRACS Institute, Ltd. | Fargo | North Dakota | 58102 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00865943, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 16, 2010 · Synced May 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00865943 live on ClinicalTrials.gov.