Rep. John E. Bradley

Filed: 10/26/2005

 

 


 

 


 
09400SB0273ham002 LRB094 04221 RLC 49960 a

1
AMENDMENT TO SENATE BILL 273

2     AMENDMENT NO. ______. Amend Senate Bill 273 by replacing
3 everything after the enacting clause with the following:
 
4     "Section 1. Short title. This Act may be cited as the
5 Methamphetamine Precursor Control Act.
 
6     Section 5. Purpose. The purpose of this Act is to reduce
7 the harm that methamphetamine manufacturing and manufacturers
8 are inflicting on individuals, families, communities, first
9 responders, the economy, and the environment in Illinois, by
10 making it more difficult for persons engaged in the unlawful
11 manufacture of methamphetamine and related activities to
12 obtain methamphetamine's essential ingredient, ephedrine or
13 pseudoephedrine.
 
14     Section 10. Definitions. In this Act:
15     "Administer" or "administration" has the meaning provided
16 in Section 102 of the Illinois Controlled Substances Act.
17     "Agent" has the meaning provided in Section 102 of the
18 Illinois Controlled Substances Act.
19     "Convenience package" means any package that contains 360
20 milligrams or less of ephedrine or pseudoephedrine, their salts
21 or optical isomers, or salts of optical isomers in liquid or
22 liquid-filled capsule form.
23     "Deliver" has the meaning provided in Section 102 of the

 

 

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1 Illinois Controlled Substances Act.
2     "Dispense" has the meaning provided in Section 102 of the
3 Illinois Controlled Substances Act.
4     "Distribute" has the meaning provided in Section 102 of the
5 Illinois Controlled Substances Act.
6     "List I chemical" has the meaning provided in 21 U.S.C.
7 Section 802.
8     "Methamphetamine precursor" has the meaning provided in
9 Section 10 of the Methamphetamine Control and Community
10 Protection Act.
11     "Package" means an item packaged and marked for retail sale
12 that is not designed to be further broken down or subdivided
13 for the purpose of retail sale.
14     "Pharmacist" has the meaning provided in Section 102 of the
15 Illinois Controlled Substances Act.
16     "Pharmacy" has the meaning provided in Section 102 of the
17 Illinois Controlled Substances Act.
18     "Practitioner" has the meaning provided in Section 102 of
19 the Illinois Controlled Substances Act.
20     "Prescriber" has the meaning provided in Section 102 of the
21 Illinois Controlled Substances Act.
22     "Prescription" has the meaning provided in Section 102 of
23 the Illinois Controlled Substances Act.
24     "Readily retrievable" has the meaning provided in 21 C.F.R.
25 part 1300.
26     "Retail distributor" means a grocery store, general
27 merchandise store, drug store, other merchandise store, or
28 other entity or person whose activities as a distributor
29 relating to drug products containing targeted methamphetamine
30 precursor are limited exclusively or almost exclusively to
31 sales for personal use by an ultimate user, both in number of
32 sales and volume of sales, either directly to walk-in customers
33 or in face-to-face transactions by direct sales.
34     "Sales employee" means any employee or agent who at any

 

 

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1 time (a) operates a cash register at which targeted packages
2 may be sold, (b) works at or behind a pharmacy counter, (c)
3 stocks shelves containing targeted packages, or (d) trains or
4 supervises any other employee or agent who engages in any of
5 the preceding activities.
6     "Single retail transaction" means a sale by a retail
7 distributor to a specific customer at a specific time.
8     "Targeted methamphetamine precursor" means any compound,
9 mixture, or preparation that contains any detectable quantity
10 of ephedrine or pseudoephedrine, their salts or optical
11 isomers, or salts of optical isomers.
12     "Targeted package" means a package, including a
13 convenience package, containing any amount of targeted
14 methamphetamine precursor.
15     "Ultimate user" has the meaning provided in Section 102 of
16 the Illinois Controlled Substances Act.
 
17     Section 15. Basic provisions.
18     (a) No targeted methamphetamine precursor shall be
19 purchased, received, or otherwise acquired in any manner other
20 than that described in Section 20 of this Act.
21     (b) No targeted methamphetamine precursor shall be
22 knowingly administered, dispensed, or distributed for any
23 purpose other than a medical purpose.
24     (c) No targeted methamphetamine precursor shall be
25 knowingly administered, dispensed, or distributed for the
26 purpose of violating or evading this Act, the Illinois
27 Controlled Substances Act, or the Methamphetamine Control and
28 Community Protection Act.
29     (d) No targeted methamphetamine precursor shall be
30 administered, dispensed, or distributed with knowledge that it
31 will be used to manufacture methamphetamine or with reckless
32 disregard of its likely use to manufacture methamphetamine.
33     (e) No targeted methamphetamine precursor shall be

 

 

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1 administered, dispensed, or distributed except by:
2         (1) a pharmacist pursuant to the valid order of a
3     prescriber;
4         (2) any other practitioner authorized to do so by the
5     Illinois Controlled Substances Act;
6         (3) a drug abuse treatment program, pursuant to
7     subsection (d) of Section 313 of the Illinois Controlled
8     Substances Act;
9         (4) a pharmacy pursuant to Section 25 of this Act;
10         (5) a retail distributor pursuant to Sections 30 and 35
11     of this Act; or
12         (6) a distributor authorized by the Drug Enforcement
13     Administration to distribute bulk quantities of a list I
14     chemical under the federal Controlled Substances Act and
15     corresponding regulations, or the employee or agent of such
16     a distributor acting in the normal course of business.
 
17     Section 20. Restrictions on purchase, receipt, or
18 acquisition.
19     (a) Except as provided in subsection (e) of this Section,
20 any person 18 years of age or older wishing to purchase,
21 receive, or otherwise acquire a targeted methamphetamine
22 precursor shall, prior to taking possession of the targeted
23 methamphetamine precursor:
24         (1) provide a driver's license or other
25     government-issued identification showing the person's
26     name, date of birth, and photograph; and
27         (2) sign a log documenting the name and address of the
28     person, date and time of the transaction, and brand and
29     product name and total quantity distributed of ephedrine or
30     pseudoephedrine, their salts, or optical isomers, or salts
31     of optical isomers.
32     (b) Except as provided in subsection (e) of this Section,
33 no person shall knowingly purchase, receive, or otherwise

 

 

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1 acquire, within any 30-day period products containing more than
2 a total of 7,500 milligrams of ephedrine or pseudoephedrine,
3 their salts or optical isomers, or salts of optical isomers.
4     (c) Except as provided in subsections (d) and (e) of this
5 Section, no person shall knowingly purchase, receive, or
6 otherwise acquire more than 2 targeted packages in a single
7 retail transaction.
8     (d) Except as provided in subsection (e) of this Section,
9 no person shall knowingly purchase, receive, or otherwise
10 acquire more than one convenience package in a 24-hour period.
11     (e) This Section shall not apply to any person who
12 purchases, receives, or otherwise acquires a targeted
13 methamphetamine precursor for the purpose of dispensing,
14 distributing, or administering it in a lawful manner described
15 in subsection (e) of Section 15 of this Act.
 
16     Section 25. Pharmacies.
17     (a) No targeted methamphetamine precursor may be knowingly
18 distributed through a pharmacy, including a pharmacy located
19 within, owned by, operated by, or associated with a retail
20 distributor unless all terms of this Section are satisfied.
21     (b) The targeted methamphetamine precursor shall:
22         (1) be packaged in blister packs, with each blister
23     containing not more than 2 dosage units, or when the use of
24     blister packs is technically infeasible, in unit dose
25     packets; and
26         (2) contain no more than 3,000 milligrams of ephedrine
27     or pseudoephedrine, their salts or optical isomers, or
28     salts of optical isomers.
29     (c) The targeted methamphetamine precursor shall be stored
30 behind the pharmacy counter and distributed by a pharmacist or
31 pharmacy technician licensed under the Pharmacy Practice Act of
32 1987.
33     (d) Any retail distributor operating a pharmacy, and any

 

 

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1 pharmacist or pharmacy technician involved in the transaction
2 or transactions, shall ensure that any person purchasing,
3 receiving, or otherwise acquiring the targeted methamphetamine
4 precursor complies with subsection (a) of Section 20 of this
5 Act.
6     (e) Any retail distributor operating a pharmacy, and any
7 pharmacist or pharmacy technician involved in the transaction
8 or transactions, shall verify that:
9         (1) The person purchasing, receiving, or otherwise
10     acquiring the targeted methamphetamine precursor is 18
11     years of age or older and resembles the photograph of the
12     person on the government-issued identification presented
13     by the person; and
14         (2) The name entered into the log referred to in
15     subsection (a) of Section 20 of this Act corresponds to the
16     name on the government-issued identification presented by
17     the person.
18     (f) The logs referred to in subsection (a) of Section 20 of
19 this Act shall be kept confidential, maintained for not less
20 than 2 years, and made available for inspection and copying by
21 any law enforcement officer upon request of that officer. These
22 logs may be kept in an electronic format if they include all
23 the information specified in subsection (a) of Section 20 of
24 this Act in a manner that is readily retrievable and
25 reproducible in hard-copy format.
26     (g) No retail distributor operating a pharmacy, and no
27 pharmacist or pharmacy technician, shall knowingly distribute
28 any targeted methamphetamine precursor to any person under 18
29 years of age.
30     (h) No retail distributor operating a pharmacy, and no
31 pharmacist or pharmacy technician, shall knowingly distribute
32 to a single person in any 24-hour period more than one
33 convenience package.
34     (i) Except as provided in subsection (h) of this Section,

 

 

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1 no retail distributor operating a pharmacy, and no pharmacist
2 or pharmacy technician, shall knowingly distribute to a single
3 person more than 2 targeted packages in a single retail
4 transaction.
5     (j) No retail distributor operating a pharmacy, and no
6 pharmacist or pharmacy technician, shall knowingly distribute
7 to a single person in any 30-day period products containing
8 more than a total of 7,500 milligrams of ephedrine or
9 pseudoephedrine, their salts or optical isomers, or salts of
10 optical isomers.
 
11     Section 30. Retail distributors; general requirements.
12     (a) No retail distributor shall distribute any convenience
13 package except in accordance with this Section and Section 35
14 of this Act.
15     (b) The convenience packages must be displayed behind store
16 counters or in locked cases, so that customers are not able to
17 reach the product without the assistance of a store employee or
18 agent.
19     (c) The retailer distributor shall ensure that any person
20 purchasing, receiving, or otherwise acquiring the targeted
21 methamphetamine precursor complies with subsection (a) of
22 Section 20 of this Act.
23     (d) The retail distributor shall verify that:
24         (1) The person purchasing, receiving, or otherwise
25     acquiring the targeted methamphetamine precursor is 18
26     years of age or older and resembles the photograph of the
27     person on the government-issued identification presented
28     by the person; and
29         (2) The name entered into the log referred to in
30     subsection (a) of Section 20 of this Act corresponds to the
31     name on the government-issued identification presented by
32     the person.
33     (e) The logs referred to in subsection (a) of Section 20 of

 

 

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1 this Act shall be kept confidential, maintained for not less
2 than 2 years, and made available for inspection and copying by
3 any law enforcement officer upon request of that officer. These
4 logs may be kept in an electronic format if they include all
5 the information specified in subsection (a) of Section 20 of
6 this Act in a form that is readily retrievable.
7     (f) No retail distributor shall knowingly distribute any
8 targeted methamphetamine precursor to any person under 18 years
9 of age.
10     (g) No retail distributor shall knowingly distribute to a
11 single person in any 24-hour period more than one convenience
12 package.
13     (h) No retail distributor shall knowingly distribute to a
14 single person in any 30-day period products containing more
15 than a total of 7,500 milligrams of ephedrine or
16 pseudoephedrine, their salts or optical isomers, or salts of
17 optical isomers.
 
18     Section 35. Retail distributors; training requirements.
19     (a) Every retail distributor of any targeted
20 methamphetamine precursor shall train each sales employee on
21 the topics listed on the certification form described in
22 subsection (b) of this Section. This training may be conducted
23 by a live trainer or by means of a computer-based training
24 program. This training shall be completed within 30 days of the
25 effective date of this Act or within 30 days of the date that
26 each sales employee begins working for the retail distributor,
27 whichever of these 2 dates comes later.
28     (b) Immediately after training each sales employee as
29 required in subsection (a) of this Section, every retail
30 distributor of any targeted methamphetamine precursor shall
31 have each sales employee read, sign, and date a certification
32 containing the following language:
33         (1) My name is (insert name of employee) and I am an

 

 

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1     employee of (insert name of business) at (insert street
2     address).
3         (2) I understand that in Illinois there are laws
4     governing the sale of certain over-the-counter medications
5     that contain a chemical called ephedrine or a second
6     chemical called pseudoephedrine. Medications that are
7     subject to these laws are called "targeted methamphetamine
8     precursors".
9         (3) I understand that "targeted methamphetamine
10     precursors" can be used to manufacture the illegal and
11     dangerous drug methamphetamine and that methamphetamine is
12     causing great harm to individuals, families, communities,
13     the economy, and the environment throughout Illinois.
14         (4) I understand that under Illinois law, unless they
15     are at a pharmacy counter, customers can only purchase
16     small "convenience packages" of "targeted methamphetamine
17     precursors".
18         (5) I understand that under Illinois law, customers can
19     only purchase these "convenience packages" if they are 18
20     years of age or older, show identification, and sign a log
21     according to procedures that have been described to me.
22         (6) I understand that under Illinois law, I cannot sell
23     more than one "convenience package" to a single customer in
24     one 24-hour period.
25         (7) I understand that under Illinois law, I cannot sell
26     "targeted methamphetamine precursors" to a person if I know
27     that the person is going to use them to make
28     methamphetamine.
29         (8) I understand that there are a number of ingredients
30     that are used to make the illegal drug methamphetamine,
31     including "targeted methamphetamine precursors" sold in
32     "convenience packages". My employer has shown me a list of
33     these various ingredients, and I have reviewed the list.
34         (9) I understand that there are certain procedures that

 

 

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1     I should follow if I suspect that a store customer is
2     purchasing "targeted methamphetamine precursors" or other
3     products for the purpose of manufacturing methamphetamine.
4     These procedures have been described to me, and I
5     understand them.
6     (c) A certification form of the type described in
7 subsection (b) of this Section may be signed with a handwritten
8 signature or an electronic signature that includes a unique
9 identifier for each employee. The certification shall be
10 retained by the retail distributor for each sales employee for
11 the duration of his or her employment and for at least 30 days
12 following the end of his or her employment. Any such form shall
13 be made available for inspection and copying by any law
14 enforcement officer upon request of that officer. These records
15 may be kept in electronic format if they include all the
16 information specified in this Section in a manner that is
17 readily retrievable and reproducible in hard-copy format.
18     (d) The Office of the Illinois Attorney General shall make
19 available to retail distributors the list of methamphetamine
20 ingredients referred to in subsection (b) of this Section.
 
21     Section 40. Penalties.
22     (a) Any pharmacy or retail distributor that violates this
23 Act is guilty of a petty offense and subject to a fine of $500
24 for a first offense; and $1,000 for a second offense occurring
25 at the same retail location as and within 3 years of the prior
26 offense. A pharmacy or retail distributor that violates this
27 Act is guilty of a business offense and subject to a fine of
28 $5,000 for a third or subsequent offense occurring at the same
29 retail location as and within 3 years of the prior offenses.
30     (b) An employee or agent of a pharmacy or retail
31 distributor who violates this Act is guilty of a Class A
32 misdemeanor for a first offense, a Class 4 felony for a second
33 offense, and a Class 1 felony for a third or subsequent

 

 

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1 offense.
2     (c) Any other person who violates this Act is guilty of a
3 Class B misdemeanor for a first offense, a Class A misdemeanor
4 for a second offense, and a Class 4 felony for a third or
5 subsequent offense.
 
6     Section 45. Immunity from civil liability. In the event
7 that any agent or employee of a pharmacy or retail distributor
8 reports to any law enforcement officer or agency any suspicious
9 activity concerning a targeted methamphetamine precursor or
10 other methamphetamine ingredient or ingredients, the agent or
11 employee and the pharmacy or retail distributor itself are
12 immune from civil liability based on allegations of defamation,
13 libel, slander, false arrest, or malicious prosecution, or
14 similar allegations, except in cases of willful or wanton
15 misconduct.
 
16     Section 50. Scope of Act.
17     (a) Nothing in this Act limits the scope, terms, or effect
18 of the Methamphetamine Control and Community Protection Act.
19     (b) Nothing in this Act limits the lawful authority granted
20 by the Medical Practice Act of 1987, the Nursing and Advanced
21 Practice Nursing Act, or the Pharmacy Practice Act of 1987.
22     (c) Nothing in this Act limits the authority or activity of
23 any law enforcement officer acting within the scope of his or
24 her employment.
 
25     Section 55. Preemption and home rule powers.
26     (a) Except as provided in subsection (b) of this Section, a
27 county or municipality, including a home rule unit, may
28 regulate the sale of targeted methamphetamine precursor and
29 targeted packages in a manner that is not more or less
30 restrictive than the regulation by the State under this Act.
31 This Section is a limitation under subsection (i) of Section 6

 

 

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1 of Article VII of the Illinois Constitution on the concurrent
2 exercise by home rule units of the powers and functions
3 exercised by the State.
4     (b) Any regulation of the sale of targeted methamphetamine
5 precursor and targeted packages by a home rule unit that took
6 effect on or before May 1, 2004, is exempt from the provisions
7 of subsection (a) of this Section.
 
8     Section 900. The Illinois Controlled Substances Act is
9 amended by changing Sections 211, 212, 216, 304, and 312 as
10 follows:
 
11     (720 ILCS 570/211)  (from Ch. 56 1/2, par. 1211)
12     Sec. 211. The Department shall issue a rule scheduling a
13 substance in Schedule V if it finds that:
14     (1) the substance has low potential for abuse relative to
15 the controlled substances listed in Schedule IV;
16     (2) the substance has currently accepted medical use in
17 treatment in the United States; and
18     (3) abuse of the substance may lead to limited
19 physiological dependence or psychological dependence relative
20 to the substances in Schedule IV, or the substance is a
21 targeted methamphetamine precursor as defined in the
22 Methamphetamine Precursor Control Act.
23 (Source: P.A. 83-969.)
 
24     (720 ILCS 570/212)  (from Ch. 56 1/2, par. 1212)
25     Sec. 212. (a) The controlled substances listed in this
26 section are included in Schedule V.
27     (b) Any compound, mixture, or preparation containing
28 limited quantities of any of the following narcotic drugs, or
29 their salts calculated as the free anhydrous base or alkaloid
30 which also contains one or more non-narcotic active medicinal
31 ingredients in sufficient proportion to confer upon the

 

 

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1 compound, mixture, or preparation, valuable medicinal
2 qualities other than those possessed by the narcotic drug alone
3 as set forth below:
4         (1) not more than 200 milligrams of codeine, or any of
5     its salts, per 100 milliliters or per 100 grams;
6         (2) not more than 100 milligrams of dihydrocodeine; or
7     any of its salts, per 100 milliliters or per 100 grams;
8         (3) not more than 100 milligrams of ethylmorphine, or
9     any of its salts, per 100 milliliters or per 100 grams;
10         (4) not more than 2.5 milligrams of diphenoxylate and
11     not less than 25 micrograms of atropine sulfate per dosage
12     unit;
13         (5) not more than 100 milligrams of opium per 100
14     milliliters or per 100 grams;
15         (6) not more than 0.5 milligram of difenoxin (DEA Drug
16     Code No. 9618) and not less than 25 micrograms of atropine
17     sulfate per dosage unit.
18     (c) Buprenorphine.
19     (d) Pyrovalerone.
20     (d-5) Any targeted methamphetamine precursor as defined in
21 the Methamphetamine Precursor Control Act.
22     (e) Any compound, mixture or preparation which contains any
23 quantity of any controlled substance when such compound,
24 mixture or preparation is not otherwise controlled in Schedules
25 I, II, III or IV.
26 (Source: P.A. 89-202, eff. 10-1-95.)
 
27     (720 ILCS 570/216)
28     Sec. 216. Ephedrine.
29     (a) The following drug products containing ephedrine, its
30 salts, optical isomers and salts of optical isomers shall be
31 exempt from the application of Sections 312 and 313 of this Act
32 if they: (i) may lawfully be sold over-the-counter without a
33 prescription under the Federal Food, Drug, and Cosmetic Act;

 

 

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1 (ii) are labeled and marketed in a manner consistent with
2 Section 341.76 of Title 21 of the Code of Federal Regulations;
3 (iii) are manufactured and distributed for legitimate
4 medicinal use in a manner that reduces or eliminates the
5 likelihood of abuse; and (iv) are not marketed, advertised, or
6 labeled for the indications of stimulation, mental alertness,
7 weight loss, muscle enhancement, appetite control, or energy:
8         (1) Solid oral dosage forms, including soft gelatin
9     caplets, which are formulated pursuant to 21 CFR 341 or its
10     successor, and packaged in blister packs of not more than 2
11     tablets per blister.
12         (2) Anorectal preparations containing not more than 5%
13     ephedrine.
14     (b) The marketing, advertising, or labeling of any product
15 containing ephedrine, a salt of ephedrine, an optical isomer of
16 ephedrine, or a salt of an optical isomer of ephedrine, for the
17 indications of stimulation, mental alertness, weight loss,
18 appetite control, or energy, is prohibited. In determining
19 compliance with this requirement the Department may consider
20 the following factors:
21         (1) The packaging of the drug product;
22         (2) The name and labeling of the product;
23         (3) The manner of distribution, advertising, and
24     promotion of the product;
25         (4) Verbal representations made concerning the
26     product;
27         (5) The duration, scope, and significance of abuse or
28     misuse of the particular product.
29     (c) A violation of this Section is a Class A misdemeanor. A
30 second or subsequent violation of this Section is a Class 4
31 felony.
32     (d) This Section does not apply to dietary supplements,
33 herbs, or other natural products, including concentrates or
34 extracts, which:

 

 

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1         (1) are not otherwise prohibited by law; and
2         (2) may contain naturally occurring ephedrine,
3     ephedrine alkaloids, or pseudoephedrine, or their salts,
4     isomers, or salts of isomers, or a combination of these
5     substances, that:
6             (i) are contained in a matrix of organic material;
7         and
8             (ii) do not exceed 15% of the total weight of the
9         natural product.
10     (e) Nothing in this Section limits the scope or terms of
11 the Methamphetamine Precursor Control Act.
12 (Source: P.A. 90-775, eff. 1-1-99.)
 
13     (720 ILCS 570/304)  (from Ch. 56 1/2, par. 1304)
14     Sec. 304. (a) A registration under Section 303 to
15 manufacture, distribute, or dispense a controlled substance or
16 purchase, store, or administer euthanasia drugs may be
17 suspended or revoked by the Department of Professional
18 Regulation upon a finding that the registrant:
19         (1) has furnished any false or fraudulent material
20     information in any application filed under this Act; or
21         (2) has been convicted of a felony under any law of the
22     United States or any State relating to any controlled
23     substance; or
24         (3) has had suspended or revoked his Federal
25     registration to manufacture, distribute, or dispense
26     controlled substances or purchase, store, or administer
27     euthanasia drugs; or
28         (4) has been convicted of bribery, perjury, or other
29     infamous crime under the laws of the United States or of
30     any State; or
31         (5) has violated any provision of this Act or any rules
32     promulgated hereunder, or any provision of the
33     Methamphetamine Precursor Control Act or rules promulgated

 

 

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1     thereunder, whether or not he has been convicted of such
2     violation; or
3         (6) has failed to provide effective controls against
4     the diversion of controlled substances in other than
5     legitimate medical, scientific or industrial channels.
6     (b) The Department of Professional Regulation may limit
7 revocation or suspension of a registration to the particular
8 controlled substance with respect to which grounds for
9 revocation or suspension exist.
10     (c) The Department of Professional Regulation shall
11 promptly notify the Administration, the Department and the
12 Department of State Police or their successor agencies, of all
13 orders denying, suspending or revoking registration, all
14 forfeitures of controlled substances, and all final court
15 dispositions, if any, of such denials, suspensions,
16 revocations or forfeitures.
17     (d) If Federal registration of any registrant is suspended,
18 revoked, refused renewal or refused issuance, then the
19 Department of Professional Regulation shall issue a notice and
20 conduct a hearing in accordance with Section 305 of this Act.
21 (Source: P.A. 93-626, eff. 12-23-03.)
 
22     (720 ILCS 570/312)  (from Ch. 56 1/2, par. 1312)
23     Sec. 312. Requirements for dispensing controlled
24 substances.
25     (a) A practitioner, in good faith, may dispense a Schedule
26 II controlled substance, which is a narcotic drug listed in
27 Section 206 of this Act; or which contains any quantity of
28 amphetamine or methamphetamine, their salts, optical isomers
29 or salts of optical isomers; phenmetrazine and its salts; or
30 pentazocine; and Schedule III, IV, or V controlled substances
31 to any person upon a written prescription of any prescriber,
32 dated and signed by the person prescribing on the day when
33 issued and bearing the name and address of the patient for

 

 

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1 whom, or the owner of the animal for which the controlled
2 substance is dispensed, and the full name, address and registry
3 number under the laws of the United States relating to
4 controlled substances of the prescriber, if he is required by
5 those laws to be registered. If the prescription is for an
6 animal it shall state the species of animal for which it is
7 ordered. The practitioner filling the prescription shall write
8 the date of filling and his own signature on the face of the
9 written prescription. The written prescription shall be
10 retained on file by the practitioner who filled it or pharmacy
11 in which the prescription was filled for a period of 2 years,
12 so as to be readily accessible for inspection or removal by any
13 officer or employee engaged in the enforcement of this Act.
14 Whenever the practitioner's or pharmacy's copy of any
15 prescription is removed by an officer or employee engaged in
16 the enforcement of this Act, for the purpose of investigation
17 or as evidence, such officer or employee shall give to the
18 practitioner or pharmacy a receipt in lieu thereof. A
19 prescription for a Schedule II controlled substance shall not
20 be filled more than 7 days after the date of issuance. A
21 written prescription for Schedule III, IV or V controlled
22 substances shall not be filled or refilled more than 6 months
23 after the date thereof or refilled more than 5 times unless
24 renewed, in writing, by the prescriber.
25     (b) In lieu of a written prescription required by this
26 Section, a pharmacist, in good faith, may dispense Schedule
27 III, IV, or V substances to any person either upon receiving a
28 facsimile of a written, signed prescription transmitted by the
29 prescriber or the prescriber's agent or upon a lawful oral
30 prescription of a prescriber which oral prescription shall be
31 reduced promptly to writing by the pharmacist and such written
32 memorandum thereof shall be dated on the day when such oral
33 prescription is received by the pharmacist and shall bear the
34 full name and address of the ultimate user for whom, or of the

 

 

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1 owner of the animal for which the controlled substance is
2 dispensed, and the full name, address, and registry number
3 under the law of the United States relating to controlled
4 substances of the prescriber prescribing if he is required by
5 those laws to be so registered, and the pharmacist filling such
6 oral prescription shall write the date of filling and his own
7 signature on the face of such written memorandum thereof. The
8 facsimile copy of the prescription or written memorandum of the
9 oral prescription shall be retained on file by the proprietor
10 of the pharmacy in which it is filled for a period of not less
11 than two years, so as to be readily accessible for inspection
12 by any officer or employee engaged in the enforcement of this
13 Act in the same manner as a written prescription. The facsimile
14 copy of the prescription or oral prescription and the written
15 memorandum thereof shall not be filled or refilled more than 6
16 months after the date thereof or be refilled more than 5 times,
17 unless renewed, in writing, by the prescriber.
18     (c) Except for any targeted methamphetamine precursor as
19 defined in the Methamphetamine Precursor Control Act, a A
20 controlled substance included in Schedule V shall not be
21 distributed or dispensed other than for a medical purpose and
22 not for the purpose of evading this Act, and then:
23         (1) only personally by a person registered to dispense
24     a Schedule V controlled substance and then only to his
25     patients, or
26         (2) only personally by a pharmacist, and then only to a
27     person over 21 years of age who has identified himself to
28     the pharmacist by means of 2 positive documents of
29     identification.
30         (3) the dispenser shall record the name and address of
31     the purchaser, the name and quantity of the product, the
32     date and time of the sale, and the dispenser's signature.
33         (4) no person shall purchase or be dispensed more than
34     120 milliliters or more than 120 grams of any Schedule V

 

 

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1     substance which contains codeine, dihydrocodeine, or any
2     salts thereof, or ethylmorphine, or any salts thereof, in
3     any 96 hour period. The purchaser shall sign a form,
4     approved by the Department of Professional Regulation,
5     attesting that he has not purchased any Schedule V
6     controlled substances within the immediately preceding 96
7     hours.
8         (5) a copy of the records of sale, including all
9     information required by paragraph (3), shall be forwarded
10     to the Department of Professional Regulation at its
11     principal office by the 15th day of the following month.
12         (6) all records of purchases and sales shall be
13     maintained for not less than 2 years.
14         (7) no person shall obtain or attempt to obtain within
15     any consecutive 96 hour period any Schedule V substances of
16     more than 120 milliliters or more than 120 grams containing
17     codeine, dihydrocodeine or any of its salts, or
18     ethylmorphine or any of its salts. Any person obtaining any
19     such preparations or combination of preparations in excess
20     of this limitation shall be in unlawful possession of such
21     controlled substance.
22         (8) a person qualified to dispense controlled
23     substances under this Act and registered thereunder shall
24     at no time maintain or keep in stock a quantity of Schedule
25     V controlled substances defined and listed in Section 212
26     (b) (1), (2) or (3) in excess of 4.5 liters for each
27     substance; a pharmacy shall at no time maintain or keep in
28     stock a quantity of Schedule V controlled substances as
29     defined in excess of 4.5 liters for each substance, plus
30     the additional quantity of controlled substances necessary
31     to fill the largest number of prescription orders filled by
32     that pharmacy for such controlled substances in any one
33     week in the previous year. These limitations shall not
34     apply to Schedule V controlled substances which Federal law

 

 

09400SB0273ham002 - 20 - LRB094 04221 RLC 49960 a

1     prohibits from being dispensed without a prescription.
2         (9) no person shall distribute or dispense butyl
3     nitrite for inhalation or other introduction into the human
4     body for euphoric or physical effect.
5     (d) Every practitioner shall keep a record of controlled
6 substances received by him and a record of all such controlled
7 substances administered, dispensed or professionally used by
8 him otherwise than by prescription. It shall, however, be
9 sufficient compliance with this paragraph if any practitioner
10 utilizing controlled substances listed in Schedules III, IV and
11 V shall keep a record of all those substances dispensed and
12 distributed by him other than those controlled substances which
13 are administered by the direct application of a controlled
14 substance, whether by injection, inhalation, ingestion, or any
15 other means to the body of a patient or research subject. A
16 practitioner who dispenses, other than by administering, a
17 controlled substance in Schedule II, which is a narcotic drug
18 listed in Section 206 of this Act, or which contains any
19 quantity of amphetamine or methamphetamine, their salts,
20 optical isomers or salts of optical isomers, pentazocine, or
21 methaqualone shall do so only upon the issuance of a written
22 prescription blank by a prescriber.
23     (e) Whenever a manufacturer distributes a controlled
24 substance in a package prepared by him, and whenever a
25 wholesale distributor distributes a controlled substance in a
26 package prepared by him or the manufacturer, he shall securely
27 affix to each package in which that substance is contained a
28 label showing in legible English the name and address of the
29 manufacturer, the distributor and the quantity, kind and form
30 of controlled substance contained therein. No person except a
31 pharmacist and only for the purposes of filling a prescription
32 under this Act, shall alter, deface or remove any label so
33 affixed.
34     (f) Whenever a practitioner dispenses any controlled

 

 

09400SB0273ham002 - 21 - LRB094 04221 RLC 49960 a

1 substance except a non-prescription targeted methamphetamine
2 precursor as defined in the Methamphetamine Precursor Control
3 Act, he shall affix to the container in which such substance is
4 sold or dispensed, a label indicating the date of initial
5 filling, the practitioner's name and address, the name of the
6 patient, the name of the prescriber, the directions for use and
7 cautionary statements, if any, contained in any prescription or
8 required by law, the proprietary name or names or the
9 established name of the controlled substance, and the dosage
10 and quantity, except as otherwise authorized by regulation by
11 the Department of Professional Regulation. No person shall
12 alter, deface or remove any label so affixed.
13     (g) A person to whom or for whose use any controlled
14 substance has been prescribed or dispensed by a practitioner,
15 or other persons authorized under this Act, and the owner of
16 any animal for which such substance has been prescribed or
17 dispensed by a veterinarian, may lawfully possess such
18 substance only in the container in which it was delivered to
19 him by the person dispensing such substance.
20     (h) The responsibility for the proper prescribing or
21 dispensing of controlled substances is upon the prescriber and
22 the responsibility for the proper filling of a prescription for
23 controlled substance drugs rests with the pharmacist. An order
24 purporting to be a prescription issued to any individual, which
25 is not in the regular course of professional treatment nor part
26 of an authorized methadone maintenance program, nor in
27 legitimate and authorized research instituted by any
28 accredited hospital, educational institution, charitable
29 foundation, or federal, state or local governmental agency, and
30 which is intended to provide that individual with controlled
31 substances sufficient to maintain that individual's or any
32 other individual's physical or psychological addiction,
33 habitual or customary use, dependence, or diversion of that
34 controlled substance is not a prescription within the meaning

 

 

09400SB0273ham002 - 22 - LRB094 04221 RLC 49960 a

1 and intent of this Act; and the person issuing it, shall be
2 subject to the penalties provided for violations of the law
3 relating to controlled substances.
4     (i) A prescriber shall not preprint or cause to be
5 preprinted a prescription for any controlled substance; nor
6 shall any practitioner issue, fill or cause to be issued or
7 filled, a preprinted prescription for any controlled
8 substance.
9     (j) No person shall manufacture, dispense, deliver,
10 possess with intent to deliver, prescribe, or administer or
11 cause to be administered under his direction any anabolic
12 steroid, for any use in humans other than the treatment of
13 disease in accordance with the order of a physician licensed to
14 practice medicine in all its branches for a valid medical
15 purpose in the course of professional practice. The use of
16 anabolic steroids for the purpose of hormonal manipulation that
17 is intended to increase muscle mass, strength or weight without
18 a medical necessity to do so, or for the intended purpose of
19 improving physical appearance or performance in any form of
20 exercise, sport, or game, is not a valid medical purpose or in
21 the course of professional practice.
22 (Source: P.A. 90-253, eff. 7-29-97; 91-576, eff. 4-1-00;
23 91-714, eff. 6-2-00.)
 
24     (720 ILCS 647/Act rep.)
25     Section 905. The Methamphetamine Precursor Retail Sale
26 Control Act is repealed.
 
27     Section 999. Effective date. This Act takes effect January
28 15, 2006.".