# To Demonstrate the Relative Bioavailability of Cefzil 250 mg/5 ml Cefprozil Oral Suspension Fed Conditions

> **NCT00881400** · PHASE1 · COMPLETED · sponsor: **Sandoz** · enrollment: 24 (actual)

## Conditions studied

- Healthy

## Interventions

- **DRUG:** Cefprozil 250 mg/5 ml Oral Suspension (Sandoz, Austria)
- **DRUG:** Cefzil (Cefprozil) 250 mg/5 ml Oral Suspension (Bristol-Myers Squibb, USA)

## Key facts

- **NCT ID:** NCT00881400
- **Lead sponsor:** Sandoz
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2004-06
- **Primary completion:** 2004-06
- **Final completion:** 2004-06
- **Target enrollment:** 24 (ACTUAL)
- **Last updated:** 2017-03-29


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00881400

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00881400, "To Demonstrate the Relative Bioavailability of Cefzil 250 mg/5 ml Cefprozil Oral Suspension Fed Conditions". Retrieved via AI Analytics 2026-09-04 from https://api.ai-analytics.org/clinical/NCT00881400. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
