Clinical Pharmacology Clinical Trial
Official title:
An Open Label Crossover Pharmacokinetic Trial of Naproxen Sodium and Diphenhydramine Hydrochloride Soft Capsules Versus Naproxen Sodium and Diphenhydramine Hydrochloride Tablets in Healthy Adult Subjects Under Fed Conditions
To evaluate the relative bioavailability of naproxen sodium/diphenhydramine hydrochloride
(DHP HCL) 220/25 mg soft capsules (Test) versus naproxen sodium/DPH HCl 220/25 mg tablets
(Reference) after a single oral administration (2 x naproxen sodium 220 mg and DPH HCl 25 mg
combination product) under fed conditions in healthy adult subjects.
To assess the safety and tolerability of the investigational products in terms of adverse
events (AEs) and clinical parameters (systolic/diastolic blood pressure, pulse rate, physical
examination, clinical and laboratory testing).
n/a
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