Transition of a solid crystalline phase to another phase having the same chemical composition but a dif- ferent crystal structure.
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Dry solid material consisting of many, usually free flowing, fine particles.
powder
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Greasy, semi-solid preparation for external application, often anhydrous, containing dissolved or dispersed medicaments.
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Liquid preparations eant for external application without friction
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Time required to achieve the minimum effective plasma concentration following administration of the dosage form.
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A Formulated preparation of molecules/drugs that are rarely if ever suitable for administration to patients without additives.
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Antibodies that makes bacteria more susceptible to phagocytosis are called ______.
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Dosage form comprising several elements (e.g., microspheres or coated pellets) dif- fering in the rate of drug release.
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Exploratory activity that begins early in pharmaceutics, involving studies designed to determine the compatibility of excipients with the active substance…
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