Public Act 104-0781
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| Public Act 104-0781 | ||||
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AN ACT concerning regulation. | ||||
Be it enacted by the People of the State of Illinois, | ||||
represented in the General Assembly: | ||||
Section 5. The Wholesale Drug Distribution Licensing Act | ||||
is amended by changing Section 56 as follows: | ||||
(225 ILCS 120/56) | ||||
(Section scheduled to be repealed on January 1, 2028) | ||||
Sec. 56. Restrictions on transactions. | ||||
(a) A licensee shall receive prescription drug returns or | ||||
exchanges from a pharmacy or other persons authorized to | ||||
administer or dispense drugs or a chain pharmacy warehouse | ||||
pursuant to the terms and conditions of the agreement between | ||||
the wholesale distributor and the pharmacy or chain pharmacy | ||||
warehouse. Returns of expired, damaged, recalled, or otherwise | ||||
non-saleable pharmaceutical products shall be distributed by | ||||
the receiving wholesale distributor only to either the | ||||
original manufacturer or a third party returns processor. | ||||
Returns or exchanges of prescription drugs, saleable or | ||||
otherwise, including any redistribution by a receiving | ||||
wholesaler, shall not be subject to the pedigree requirements | ||||
of Section 57 of this Act, so long as they are exempt from the | ||||
pedigree requirement of the FDA's currently applicable | ||||
Prescription Drug Marketing Act guidance. Both licensees under | ||||
this Act and pharmacies or other persons authorized to | ||
administer or dispense drugs shall be accountable for | ||
administering their returns process and ensuring that the | ||
aspects of this operation are secure and do not permit the | ||
entry of adulterated and counterfeit product. | ||
(b) A manufacturer or wholesale distributor licensed under | ||
this Act may furnish prescription drugs only to a person | ||
licensed by the appropriate state licensing authorities. | ||
Before furnishing prescription drugs to a person not known to | ||
the manufacturer or wholesale distributor, the manufacturer or | ||
wholesale distributor must affirmatively verify that the | ||
person is legally authorized to receive the prescription drugs | ||
by contacting the appropriate state licensing authorities. | ||
(c) Prescription drugs furnished by a manufacturer or | ||
wholesale distributor licensed under this Act may be delivered | ||
only to the business address of a licensee, to the premises | ||
listed on a the license, or, if the Department has received | ||
notice that a licensee has authorized a health care entity to | ||
receive the prescription drugs, to the address of a health | ||
care entity, provided that the manufacturer or wholesale | ||
distributor may furnish prescription drugs to an authorized | ||
person or agent of that person at the premises of the | ||
manufacturer or wholesale distributor if: | ||
(1) the identity and authorization of the recipient is | ||
properly established; and | ||
(2) this method of receipt is employed only to meet | ||
the immediate needs of a particular patient of the | ||
authorized person. | ||
Prescription drugs that are controlled substances | ||
furnished by a manufacturer or wholesale distributor licensed | ||
under this Act may be delivered only to a registered place of | ||
business or professional practice, as required by Section 302 | ||
of the Illinois Controlled Substances Act. | ||
For the purposes of this subsection (c), "health care | ||
entity" means an entity where medical, dental, or veterinary | ||
services are provided by a licensed practitioner and where the | ||
licensed practitioner is responsible for the receipt, storage, | ||
and use of drugs. | ||
(d) Prescription drugs may be furnished to a hospital | ||
pharmacy receiving area, provided that a pharmacist or | ||
authorized receiving personnel signs, at the time of delivery, | ||
a receipt showing the type and quantity of the prescription | ||
drug received. Any discrepancy between the receipt and the | ||
type and quantity of the prescription drug actually received | ||
shall be reported to the delivering manufacturer or wholesale | ||
distributor by the next business day after the delivery to the | ||
pharmacy receiving area. | ||
(e) A manufacturer or wholesale distributor licensed under | ||
this Act may not accept payment for, or allow the use of, a | ||
person or entity's credit to establish an account for the | ||
purchase of prescription drugs from any person other than the | ||
owner of record, the chief executive officer, or the chief | ||
financial officer listed on the license of a person or entity | ||
legally authorized to receive the prescription drugs. Any | ||
account established for the purchase of prescription drugs | ||
must bear the name of the licensee. This subsection (e) shall | ||
not be construed to prohibit a pharmacy or chain pharmacy | ||
warehouse from receiving prescription drugs if payment for the | ||
prescription drugs is processed through the pharmacy's or | ||
chain pharmacy warehouse's contractual drug manufacturer or | ||
wholesale distributor. | ||
(Source: P.A. 95-689, eff. 10-29-07.) | ||
Effective Date: 1/1/2027
