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...Accessed from by aptuit on sat dec est usp general information pharmaceutical dosage forms maceutical preparations which are given elsewhere in this tent uniformity does not rely the assumption of blend pharmacopeia and can be applied all cases successful devel opment manufacture requires careful evaluation api particle or droplet size incorporation tech niques excipient properties stability see also drug product involves chemical change to read physical performance over time form matrix must support expiration dating for commercially prepared a beyond use date compounded test procedures potency indicat ing validation compendial degra dation products should quantified case dis persed emulsified systems consideration potential settling separation formulation components any changes easily reversed e g shaking prior dosing ad considerations ministration example tablets capsules oral chapter provides descriptions defini suspensions vitro release such as dissolu tions commonly used tion dis...