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HB 4953

Illinois HousePassed

Summary

HB 4953, “DRUG DISTRIBUTION RESTRICTIONS”, was introduced in the House on Feb 4, 2026 by Rep. Martha Deuter (D) with 5 co-sponsors. It last saw action on Aug 7, 2026: Public Act . . . . . . . . . 104-0781.


Record

Text

HB 4953 has 5 co-sponsors and 5 roll calls.

hb4953/enrolled.txt
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Full Text of HB4953
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HB4953 - 104th General Assembly
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HB4953 Enrolled LRB104 19403 AAS 32851 b
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(Section scheduled to be repealed on January 1, 2028)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
HB4953 Enrolled - 2 - LRB104 19403 AAS 32851 b
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
HB4953 Enrolled - 3 - LRB104 19403 AAS 32851 b
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
HB4953 Enrolled - 4 - LRB104 19403 AAS 32851 b
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.)

Amends the Wholesale Drug Distribution Licensing Act. In provisions concerning restrictions on transactions, provides that prescription drugs furnished by a manufacturer or wholesale distributor licensed under the Act may be delivered only to the business address of a licensee registered with the Department of Financial and Professional Regulation, to the premises listed on a license, or, if the Department has received notice that the licensee has authorized a health care entity to receive the prescription drugs, to the address of a health care entity (instead of only to the premises listed on the license). Provides that "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.

Sponsors

Rep. Martha Deuter (D) sponsors HB 4953, and 5 members have co-sponsored it.

Committees

HB 4953 went before 4 committees: Rules, Health Care Licenses, Assignments and Licensed Activities.

Rules
Rules
Referred to · Feb 6, 2026 · 5,290 Bills
Health Care Licenses
Health Care Licenses
Referred to · Feb 17, 2026
Assignments
Assignments
Referred to · Apr 10, 2026
Licensed Activities
Licensed Activities
Referred to · May 12, 2026

History

HB 4953 has taken 40 actions since Feb 4, 2026, the latest on Aug 7, 2026.

ChamberAction
Aug 7, 2026
House
Governor Approved
Aug 7, 2026
House
Effective Date January 1, 2027
Aug 7, 2026
House
Public Act . . . . . . . . . 104-0781
Jun 26, 2026
House
Sent to the Governor
May 30, 2026
Senate
Added as Alternate Co-Sponsor Sen. Cristina Castro

Votes

HB 4953 went to 5 roll calls across both chambers, the latest on May 28, 2026 at 590.

ChamberQuestion
Yea
Nay
May 28, 2026
Senate
Senate Third Reading
59
0
May 20, 2026
Senate
Senate Licensed Activities Committee
6
0
Apr 8, 2026
House
House Third Reading
109
0
Mar 25, 2026
House
House Health Care Licenses Committee
14
0
Feb 25, 2026
House
House Health Care Licenses Committee
13
0

Source: ilga.gov · legiscan.com