DRCNet Response to the
Drug Enforcement Administration
Distribution
The keeping of records is required for distribution of a controlled substance from one
manufacturer to another, from manufacturer to distributor, and from distributor to
dispenser. In the case of Schedule I and II drugs, the supplier must have a special order
form from the customer. This order form (DEA Form 222) is issued by the DEA only to
persons who are properly registered to handle Schedules I and II. The form is preprinted
with the name and address of the customer. The drugs must be shipped to this name and
address. The use of this device is a special reinforcement of the registration
requirement; it makes doubly certain that only authorized individuals may obtain Schedule
I and II drugs. Another benefit of the form is the special monitoring it permits. The form
is issued in triplicate: the customer keeps one copy; two copies go to the supplier who,
after filling the order, keeps a copy and forwards the third copy to the nearest DEA
office.
For drugs in Schedules III, IV, and V, no order form is necessary. The supplier in each
case, however, is under an obligation to verify the authenticity of the customer. The
supplier is held fully accountable for any drugs which are shipped to a purchaser who does
not have a valid registration.
Manufacturers must submit periodic reports of the Schedule I and II controlled
substances they produce in bulk and dosage forms. They also report the manufactured
quantity and form of each narcotic substance listed in Schedules III, IV, and V, as well
asthe quantity of synthesized psychotropic substances listed in Schedules I, II, III, and
IV. Distributors of controlled substances must report the quantity and form of all their
transactions of controlled drugs listed in Schedules I and II and narcotics listed in
Schedule III. Both manufacturers and distributors are required to provide reports of their
annual inventories of these controlled substances. This data is entered into a system
called the Automated Reports and Consolidated Orders System (ARCOS). It enables the DEA to
monitorthe distribution of controlled substances throughout the country, and to identify
retail-level registrants that receive unusual quantities of controlled substances.
Travel back to the DRCNet Response to the DEA Home Page