| http://www.w3.org/ns/prov#value | - In one embodiment of the invention, the cefditoren, or a salt, derivative, prodrug, or other form thereof, when administered in the nanoparticulate composition of the present invention, has a bioavailability that is about 50% greater than the cefditoren, or a salt, derivative, prodrug, or other form thereof, when administered in a conventional dosage form.
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