The steady state is the condition when the rate of drug administration is equal to the rate of drug elimination.

When the drug is administered as a constant rate IV infusion, there will be one steady state concentration as long as the rate of administration and the rate of elimination do not change.

When drug administration involves repeated doses, the drug concentration-time profile during each of the dosing intervals ( τ ) will be identical at steady state. This means that the maximum, the minimum, and the average concentrations during each dosing interval will be similar at steady state.

Bioavailability is a measure of the fraction of the administration dose that reaches the systemic circulation.

Absolute bioavailability is the fraction of the total dose that reaches the systemic circulation. It can take values between zero when the drug is not absorbed at all to 1 when all the administered dose reaches the systemic circulation. The absolute bioavailability can be expressed in terms of percentage (0-100%).

The relative bioavailability is the bioavailability of a drug product relative to the bioavailability of another drug product (reference standard preparation). The relative bioavailability can take any value above zero. It can be more than one when the product under investigation has bioavailability higher than that of the reference standard.

The dosing interval is the period of time between administration of doses.

The first-order absorption rate constant is rate constant that determines the rate of drug absorption from the site of administration. Larger absorption rate constant results in faster rate of drug absorption.

The absorption rate constant determined after drug administration is an operative rate constant that accounts for all the necessary steps required for drug absorption into the systemic circulation including disintegration, dissolution and absorption.

The first-order absorption rate constant has units of time-1.