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Back to HB 4953
Illinois General Assembly· HB 4953Governor Approved

DRUG DISTRIBUTION RESTRICTIONS, the official text

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HB4953 Enrolled                      LRB104 19403 AAS 32851 b

1  AN ACT concerning regulation.

2  Be it enacted by the People of the State of Illinois,

3 represented in the General Assembly:

4  Section 5. The Wholesale Drug Distribution Licensing Act

5 is amended by changing Section 56 as follows:

6  (225 ILCS 120/56)

7  (Section scheduled to be repealed on January 1, 2028)

8  Sec. 56. Restrictions on transactions.

9  (a) A licensee shall receive prescription drug returns or

10 exchanges from a pharmacy or other persons authorized to

11 administer or dispense drugs or a chain pharmacy warehouse

12 pursuant to the terms and conditions of the agreement between

13 the wholesale distributor and the pharmacy or chain pharmacy

14 warehouse. Returns of expired, damaged, recalled, or otherwise

15 non-saleable pharmaceutical products shall be distributed by

16 the receiving wholesale distributor only to either the

17 original manufacturer or a third party returns processor.

18 Returns or exchanges of prescription drugs, saleable or

19 otherwise, including any redistribution by a receiving

20 wholesaler, shall not be subject to the pedigree requirements

21 of Section 57 of this Act, so long as they are exempt from the

22 pedigree requirement of the FDA's currently applicable

23 Prescription Drug Marketing Act guidance. Both licensees under
    HB4953 Enrolled  -2-       LRB104 19403 AAS 32851 b

1 this Act and pharmacies or other persons authorized to

2 administer or dispense drugs shall be accountable for

3 administering their returns process and ensuring that the

4 aspects of this operation are secure and do not permit the

5 entry of adulterated and counterfeit product.

6   (b) A manufacturer or wholesale distributor licensed under

7 this Act may furnish prescription drugs only to a person

8 licensed by the appropriate state licensing authorities.

9 Before furnishing prescription drugs to a person not known to

10 the manufacturer or wholesale distributor, the manufacturer or

11 wholesale distributor must affirmatively verify that the

12 person is legally authorized to receive the prescription drugs

13 by contacting the appropriate state licensing authorities.

14  (c) Prescription drugs furnished by a manufacturer or

15 wholesale distributor licensed under this Act may be delivered

16 only to the business address of a licensee, to the premises

17 listed on a the license, or, if the Department has received

18 notice that a licensee has authorized a health care entity to

19 receive the prescription drugs, to the address of a health

20 care entity, provided that the manufacturer or wholesale

21 distributor may furnish prescription drugs to an authorized

22 person or agent of that person at the premises of the

23 manufacturer or wholesale distributor if:

24  (1) the identity and authorization of the recipient is

25  properly established; and

26  (2) this method of receipt is employed only to meet
    HB4953 Enrolled          -3-  LRB104 19403 AAS 32851 b

1   the immediate needs of a particular patient of the

2   authorized person.

3   Prescription drugs that are controlled substances

4 furnished by a manufacturer or wholesale distributor licensed

5 under this Act may be delivered only to a registered place of

6 business or professional practice, as required by Section 302

7 of the Illinois Controlled Substances Act.

8   For the purposes of this subsection (c), "health care

9 entity" means an entity where medical, dental, or veterinary

10 services are provided by a licensed practitioner and where the

11 licensed practitioner is responsible for the receipt, storage,

12 and use of drugs.

13  (d) Prescription drugs may be furnished to a hospital

14 pharmacy receiving area, provided that a pharmacist or

15 authorized receiving personnel signs, at the time of delivery,

16 a receipt showing the type and quantity of the prescription

17 drug received. Any discrepancy between the receipt and the

18 type and quantity of the prescription drug actually received

19 shall be reported to the delivering manufacturer or wholesale

20 distributor by the next business day after the delivery to the

21 pharmacy receiving area.

22  (e) A manufacturer or wholesale distributor licensed under

23 this Act may not accept payment for, or allow the use of, a

24 person or entity's credit to establish an account for the

25 purchase of prescription drugs from any person other than the

26 owner of record, the chief executive officer, or the chief
HB4953 Enrolled  -4-  LRB104 19403 AAS 32851 b

 1 financial officer listed on the license of a person or entity
 2 legally authorized to receive the prescription drugs. Any
 3 account established for the purchase of prescription drugs
 4 must bear the name of the licensee. This subsection (e) shall
 5 not be construed to prohibit a pharmacy or chain pharmacy
 6 warehouse from receiving prescription drugs if payment for the
 7 prescription drugs is processed through the pharmacy's or
 8 chain pharmacy warehouse's contractual drug manufacturer or
 9 wholesale distributor.
10 (Source: P.A. 95-689, eff. 10-29-07.)
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