Comparison of the rate and extent of the absorption of drug from the formulation under study to the data of a reference standard that is given intravenously is known as:

Related MCQs

• How much time does an intravenously administered drug take to complete a complete circulation?
• For a certain drug, the bile flow rate is 0.7 ml/mm, the biliary drug concentration is 2g/ml and the plasma drug concentration is 0.8g/ml. What will be the bile clearance?
• Which of the following is a correct method to find the fraction of unbound drug in plasma? Given where Cu is the concentration of unbound drug and C is total plasma drug concentration.
• What will be the rate of filtration if the rate of secretion is 0.9 ml/ sec, rate of reabsorption is 0.2 ml/sec and the rate of excretion is 2ml/sec for a particular drug?
• The extent of drug-protein binding can change with both changes in protein and drug concentration.
• If the bioavailability of test formulation is 80-120% of the reference standard, it is considered to be bioequivalent.
• Which are the two rate-determining step of drug absorption when given orally?
• Absorption of drugs can be categorized into 2 classes, physicochemical properties of drugs and Dosage form of the drug, on the basis of drug dissolution.
• Which of the following creates nonlinearity in drug distribution and not in drug absorption?
• Factors altering the binding of the drug to the blood increases the volume of distribution of the drug and the factors that influence drug binding to the extravascular component decreases the volume of distribution.