Bioavailability of Prochlorperazine Suppositories, 25 mg
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The purpose of this study is to compare prochlorperazine plasma concentrations produced after administration of the test formulation with those produced after administration of a marketed reference product.
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Ages Eligible for Study:
18 Years to 50 Years (Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Good health as determined by lack of clinically significant abnormalities in health assessment performed at screening
Positive test results for HIV or Hepatitis B or C
History of allergy or sensitivity to Prochlorperazine or related drugs