Adderall is a mixture of four amphetamine salt forms — approximately 75% dextroamphetamine salts and 25% levoamphetamine salts. Dextroamphetamine has a stronger central nervous system (CNS) effect; levoamphetamine contributes more to peripheral cardiovascular effects. Both isomers are pharmacologically active immediately after absorption, giving Adderall its characteristic direct onset.
Its primary mechanism is to enter presynaptic neurons and force the release of dopamine and norepinephrine through the DAT and NET transporters running in reverse — a direct "dump" of catecholamines into the synapse. It also inhibits monoamine oxidase (MAO), the enzyme that breaks down these neurotransmitters, extending their effect. This dual action on both release and reuptake makes Adderall pharmacologically potent.
The IR formulation is shorter-acting, wearing off within several hours. Adderall XR uses a biphasic bead technology — half the beads release immediately, the other half delay — effectively approximating two IR doses from a single capsule.
Adderall is DEA Schedule II. Prescriptions cannot be phoned in — a new written or electronic prescription is required each month. Sharing, selling, or using without a prescription is a federal crime and poses significant cardiovascular and psychiatric risks.