The present study was adopted to evaluate the pharmacokinetics of sulpiride after oral administration.
The present study was adopted to evaluate the pharmacokinetics of sulpiride after administration of single oral doses of 50 mg in an open-label, one-way study.
Study Type
INTERVENTIONAL
Allocation
NA
Masking
NONE
Enrollment
16
Pharmaceutics Department, Faculty of Pharmacy, Damanhour University
Damanhur, Egypt
•Assessment of the bioequivalence of the oral suspension formulation, the oral solution formulation, and the marketed tablet formulation of levofloxacin, on Days 1, 2, and 3, using the marketed tablet as the reference. Pharmacokinetics of sulpiride
Assessment of the pharmacokinetics using compartmental and non compartmental analysis of sulpiride after oral administration
Time frame: The pharmacokinetic analysis is done after blood sampling
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