Dexmethylphenidate Hydrochloride Tablets Under Fasting Conditions
Status:
Completed
Trial end date:
2004-06-01
Target enrollment:
Participant gender:
Summary
The objective of this randomized, single-dose, two-way evaluation is to compare the
bioequivalence of a test dexmethylphenidate hydrochloride formulation to an equivalent oral
dose of the commercially available dexmethylphenidate hydrochloride in a test population of
24 adult subjects under fasted conditions.