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Clinical Trial Summary

Determine and compare the plasma concentrations and safety and tolerability of Guaifenesin and hydrocodone bitartrate when they are administered alone or in combination to normal healthy male and/or female subjects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03642873
Study type Interventional
Source Reckitt Benckiser LLC
Contact
Status Completed
Phase Phase 1
Start date May 5, 2007
Completion date May 21, 2007

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