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[55] [7] [9] [12] The bioavailability of the oral form of selegiline is 4 to 10%, [5] [11] [12] of the ODT is 5 to 8 times that of the oral form, [13] [7] [14] and of the transdermal patch is 75%. [9] The time to peak levels of selegiline with oral administration is about 0.5 to 1.5 hours. [5] The plasma protein binding of selegiline is 85 to 90%.
MPA is available alone in the form of 2.5, 5, and 10 mg oral tablets, as a 150 mg/mL (1 mL) or 400 mg/mL (2.5 mL) microcrystalline aqueous suspension for intramuscular injection, and as a 104 mg (0.65 mL of 160 mg/mL) microcrystalline aqueous suspension for subcutaneous injection.
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