Bill Text: IL SB3502 | 2013-2014 | 98th General Assembly | Introduced
NOTE: There are more recent revisions of this legislation. Read Latest Draft
Bill Title: Amends the Illinois Controlled Substances Act. Provides that substances containing ephedrine or pseudoephedrine, their salts or optical isomers, or salts of optical isomers, are Schedule III controlled substances and require a prescription.
Spectrum: Partisan Bill (Democrat 1-0)
Status: (Failed) 2015-01-13 - Session Sine Die [SB3502 Detail]
Download: Illinois-2013-SB3502-Introduced.html
Bill Title: Amends the Illinois Controlled Substances Act. Provides that substances containing ephedrine or pseudoephedrine, their salts or optical isomers, or salts of optical isomers, are Schedule III controlled substances and require a prescription.
Spectrum: Partisan Bill (Democrat 1-0)
Status: (Failed) 2015-01-13 - Session Sine Die [SB3502 Detail]
Download: Illinois-2013-SB3502-Introduced.html
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1 | AN ACT concerning criminal law.
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2 | Be it enacted by the People of the State of Illinois,
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3 | represented in the General Assembly:
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4 | Section 5. The Illinois Controlled Substances Act is | |||||||||||||||||||
5 | amended by changing Section 208 as follows:
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6 | (720 ILCS 570/208) (from Ch. 56 1/2, par. 1208)
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7 | Sec. 208.
(a) The controlled substances listed in this | |||||||||||||||||||
8 | Section are
included in Schedule III.
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9 | (b) Unless specifically excepted or unless listed in | |||||||||||||||||||
10 | another
schedule, any material, compound, mixture, or | |||||||||||||||||||
11 | preparation which contains
any quantity of the following | |||||||||||||||||||
12 | substances having a stimulant effect on
the central nervous | |||||||||||||||||||
13 | system, including its salts, isomers (whether
optical | |||||||||||||||||||
14 | position, or geometric), and salts of such isomers whenever the
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15 | existence of such salts, isomers, and salts of isomers is | |||||||||||||||||||
16 | possible
within the specific chemical designation;
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17 | (1) Those compounds, mixtures, or preparations in | |||||||||||||||||||
18 | dosage unit form
containing any stimulant substances | |||||||||||||||||||
19 | listed in Schedule II which
compounds, mixtures, or | |||||||||||||||||||
20 | preparations were listed on August 25, 1971, as
excepted | |||||||||||||||||||
21 | compounds under Title 21, Code of Federal Regulations, | |||||||||||||||||||
22 | Section
308.32, and any other drug of the quantitative | |||||||||||||||||||
23 | composition shown in that
list for those drugs or which is |
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1 | the same except that it contains a
lesser quantity of | ||||||
2 | controlled substances;
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3 | (2) Benzphetamine;
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4 | (3) Chlorphentermine;
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5 | (4) Clortermine;
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6 | (5) Phendimetrazine.
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7 | (c) Unless specifically excepted or unless listed in | ||||||
8 | another
schedule, any material, compound, mixture, or | ||||||
9 | preparation which contains
any quantity of the following | ||||||
10 | substances having a potential for abuse
associated with a | ||||||
11 | depressant effect on the central nervous system:
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12 | (1) Any compound, mixture, or preparation containing | ||||||
13 | amobarbital,
secobarbital, pentobarbital or any salt | ||||||
14 | thereof and one or more other
active medicinal ingredients | ||||||
15 | which are not listed in any schedule;
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16 | (2) Any suppository dosage form containing | ||||||
17 | amobarbital,
secobarbital, pentobarbital or any salt of | ||||||
18 | any of these drugs and
approved by the Federal Food and | ||||||
19 | Drug Administration for marketing only
as a suppository;
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20 | (3) Any substance which contains any quantity of a | ||||||
21 | derivative of
barbituric acid, or any salt thereof:
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22 | (3.1) Aprobarbital; | ||||||
23 | (3.2) Butabarbital (secbutabarbital); | ||||||
24 | (3.3) Butalbital; | ||||||
25 | (3.4) Butobarbital (butethal);
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26 | (4) Chlorhexadol;
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1 | (5) Methyprylon;
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2 | (6) Sulfondiethylmethane;
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3 | (7) Sulfonethylmethane;
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4 | (8) Sulfonmethane;
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5 | (9) Lysergic acid;
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6 | (10) Lysergic acid amide;
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7 | (10.1) Tiletamine or zolazepam or both, or any salt of | ||||||
8 | either of them.
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9 | Some trade or other names for a tiletamine-zolazepam
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10 | combination product: Telazol.
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11 | Some trade or other names for Tiletamine:
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12 | 2-(ethylamino)-2-(2-thienyl)-cyclohexanone.
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13 | Some trade or other names for zolazepam:
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14 | 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-
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15 | [3,4-e], [1,4]-diazepin-7(1H)-one, and flupyrazapon.
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16 | (11) Any material, compound, mixture or preparation | ||||||
17 | containing not more
than 12.5 milligrams of pentazocine or | ||||||
18 | any of its salts, per 325 milligrams of
aspirin;
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19 | (12) Any material, compound, mixture or preparation | ||||||
20 | containing not
more than 12.5 milligrams of pentazocine or | ||||||
21 | any of its salts, per 325
milligrams of acetaminophen;
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22 | (13) Any material, compound, mixture or preparation | ||||||
23 | containing not more
than 50 milligrams of pentazocine or | ||||||
24 | any of its salts plus naloxone HCl USP
0.5 milligrams, per | ||||||
25 | dosage unit;
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26 | (14) Ketamine;
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1 | (15) Thiopental. | ||||||
2 | (d) Nalorphine.
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3 | (d.5) Buprenorphine. | ||||||
4 | (e) Unless specifically excepted or unless listed in | ||||||
5 | another
schedule, any material, compound, mixture, or | ||||||
6 | preparation containing
limited quantities of any of the | ||||||
7 | following narcotic drugs, or their salts
calculated as the free | ||||||
8 | anhydrous base or alkaloid, as set forth below:
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9 | (1) not more than 1.8 grams of codeine per 100
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10 | milliliters or not more than 90 milligrams per dosage unit, | ||||||
11 | with an
equal or greater quantity of an isoquinoline | ||||||
12 | alkaloid of opium;
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13 | (2) not more than 1.8 grams of codeine per 100
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14 | milliliters or not more than 90 milligrams per dosage unit, | ||||||
15 | with one or
more active non-narcotic ingredients in | ||||||
16 | recognized therapeutic amounts;
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17 | (3) not more than 300 milligrams of dihydrocodeinone | ||||||
18 | per 100 milliliters
or not more than 15 milligrams per | ||||||
19 | dosage
unit, with a fourfold or greater quantity of an | ||||||
20 | isoquinoline alkaloid of
opium;
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21 | (4) not more than 300 milligrams of dihydrocodeinone | ||||||
22 | per 100 milliliters
or not more than 15 milligrams per | ||||||
23 | dosage
unit, with one or more active, non-narcotic | ||||||
24 | ingredients in recognized
therapeutic amounts;
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25 | (5) not more than 1.8 grams of dihydrocodeine
per 100 | ||||||
26 | milliliters or not more than 90 milligrams per dosage unit, |
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1 | with
one or more active, non-narcotic ingredients in | ||||||
2 | recognized therapeutic
amounts;
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3 | (6) not more than 300 milligrams of ethylmorphine per | ||||||
4 | 100 milliliters
or not more than 15 milligrams per dosage
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5 | unit, with one or more active, non-narcotic ingredients in | ||||||
6 | recognized
therapeutic amounts;
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7 | (7) not more than 500 milligrams of opium per 100 | ||||||
8 | milliliters or per
100 grams, or not more than 25 | ||||||
9 | milligrams per dosage unit, with one or
more active, | ||||||
10 | non-narcotic ingredients in recognized therapeutic | ||||||
11 | amounts;
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12 | (8) not more than 50 milligrams of morphine
per 100 | ||||||
13 | milliliters or per 100 grams with one or more active,
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14 | non-narcotic ingredients in recognized therapeutic | ||||||
15 | amounts.
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16 | (f) Anabolic steroids, except the following anabolic | ||||||
17 | steroids that are
exempt:
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18 | (1) Androgyn L.A.;
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19 | (2) Andro-Estro 90-4;
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20 | (3) depANDROGYN;
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21 | (4) DEPO-T.E.;
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22 | (5) depTESTROGEN;
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23 | (6) Duomone;
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24 | (7) DURATESTRIN;
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25 | (8) DUO-SPAN II;
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26 | (9) Estratest;
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1 | (10) Estratest H.S.;
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2 | (11) PAN ESTRA TEST;
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3 | (12) Premarin with Methyltestosterone;
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4 | (13) TEST-ESTRO Cypionates;
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5 | (14) Testosterone Cyp 50 Estradiol Cyp 2;
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6 | (15) Testosterone Cypionate-Estradiol Cypionate | ||||||
7 | injection; and
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8 | (16) Testosterone Enanthate-Estradiol Valerate | ||||||
9 | injection.
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10 | (g) Hallucinogenic
substances.
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11 | (1) Dronabinol (synthetic) in sesame oil and | ||||||
12 | encapsulated in a soft
gelatin capsule in a U.S.
Food and | ||||||
13 | Drug Administration approved product. Some other names for
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14 | dronabinol: (6aR-trans)-6a,7,8,10a-tetrahydro-
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15 | 6,6,9-trimethyl-3-pentyl-6H-dibenzo (b,d)
pyran-1-ol) or | ||||||
16 | (-)-delta-9-(trans)-tetrahydrocannabinol.
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17 | (2) (Reserved).
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18 | (g-5) Ephedrine or pseudoephedrine, their salts or optical | ||||||
19 | isomers, or salts of optical isomers. | ||||||
20 | (h) The Department may except by rule any compound, | ||||||
21 | mixture, or
preparation containing any stimulant or depressant | ||||||
22 | substance listed in
subsection (b) from the application of all | ||||||
23 | or any part of this
Act if the compound, mixture, or | ||||||
24 | preparation contains one or more active
medicinal ingredients | ||||||
25 | not having a stimulant or depressant effect on the
central | ||||||
26 | nervous system, and if the admixtures are included therein in
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1 | combinations, quantity, proportion, or concentration that | ||||||
2 | vitiate the
potential for abuse of the substances which have a | ||||||
3 | stimulant or
depressant effect on the central nervous system.
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4 | (Source: P.A. 96-328, eff. 8-11-09; 96-1000, eff. 7-2-10; | ||||||
5 | 97-334, eff. 1-1-12.)
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