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The drug layer 30 comprises a composition formed of a liquid active agent formulation absorbed in porous particles, the preferred characteristics of the particles being described elsewhere herein, and a carrier, such as a hydrophilic polymer. The hydrophilic polymer provides a hydrophilic polymer composition in the drug layer that may contribute to the uniform release rate of active agent and controlled delivery pattern by controlling the rate of release of the porous particles containing the liquid, active agent formulation from the dosage form. Representative examples of these polymers are poly (alkylene oxide) of 100,000 to 750,000 number-average molecular weight, including poly (ethylene oxide), poly (methylene oxide), poly (butylene oxide) and poly (hexylene oxide); and a poly(carboxymethylcellulose) of 40,000 to 400,000 number-average molecular weight, represented by poly(alkali carboxymethylcellulose)poly(sodium carboxymethylcellulose), poly (potassium carboxymethylcellulose) and poly (lithium carboxymethylcellulose). The drug composition can comprise a hydroxypropylalkylcellulose of 9,200 to 125,000 number-average molecular weight for enhancing the delivery properties of the dosage form as represented by hydroxypropylethylcellulose, hydroxypropyl methylcellulose, hydroxypropylbutylcellulose and hydroxypropylpentylcellulose; and a poly (vinylpyrrolidone) of 7,000 to 75,000 number- average molecular weight for enhancing the flow properties of the dosage form.

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