2003 Legislation
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HOUSE BILL NO. 237 – Controlled substances, GHB

HOUSE BILL NO. 237

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Daily Data Tracking History



H0237....................................................by HEALTH AND WELFARE
CONTROLLED SUBSTANCES - Amends existing law to expand the description of gamma
hydroxybutyric acid and to allow gamma hydroxybutyric acid to be placed in
other schedules; to move the substance buprenorphine from Schedule V to
Schedule III and to add any drug product containing gamma hydroxybutyric acid
to Schedule III; and to include the substances listed in Section 37-2705(e),
Idaho Code, and any drug product containing gamma hydroxybutyric acid under
the penalty provisions for persons being under the influence of controlled
substances and being on a public roadway or conveyance.
                                                                        
02/11    House intro - 1st rdg - to printing
02/12    Rpt prt - to Health/Wel
02/25    Rpt out - rec d/p - to 2nd rdg
02/26    2nd rdg - to 3rd rdg
02/27    3rd rdg - PASSED - 65-0-5
      AYES -- Andersen, Barraclough, Barrett, Bauer, Bedke, Bell, Bieter,
      Black, Block, Boe, Bolz, Bradford, Campbell, Cannon, Collins, Crow,
      Cuddy, Denney, Douglas, Eberle, Edmunson, Ellsworth, Eskridge,
      Field(18), Field(23), Gagner, Garrett, Harwood, Henbest, Jaquet, Jones,
      Kulczyk, Lake, Langford, Langhorst, Martinez, McGeachin, McKague, Meyer,
      Miller, Mitchell, Moyle, Naccarato, Nielsen, Raybould, Ridinger, Ring,
      Ringo, Roberts, Robison, Rydalch, Sali, Sayler, Schaefer, Shepherd,
      Shirley, Skippen, Smith(30), Smith(24), Smylie, Snodgrass, Stevenson,
      Tilman, Wills, Wood
      NAYS -- None
      Absent and excused -- Clark, Deal, Kellogg, Trail, Mr. Speaker
    Floor Sponsor - Field(23)
    Title apvd - to Senate
02/28    Senate intro - 1st rdg - to Health/Wel
03/17    Rpt out - rec d/p - to 2nd rdg
03/19    2nd rdg - to 3rd rdg
03/20    3rd rdg - PASSED - 34-0-1
      AYES -- Andreason, Bailey, Bunderson, Burkett, Burtenshaw,
      Calabretta(Wilson), Cameron, Compton, Darrington, Davis, Gannon, Geddes,
      Goedde, Hill, Ingram, Kennedy, Keough, Little, Lodge, Malepeai, Marley,
      McKenzie, McWilliams, Noble, Noh, Pearce, Richardson, Schroeder,
      Sorensen, Stegner, Stennett, Sweet, Werk, Williams
      NAYS -- None
      Absent and excused -- Brandt
    Floor Sponsor - Burkett
    Title apvd - to House
03/21    To enrol
03/24    Rpt enrol - Sp signed
03/25    Pres signed
03/26    To Governor
03/31    Governor signed
         Session Law Chapter 185
         Effective: 07/01/03

Bill Text


                                                                        
                                                                        
  ||||              LEGISLATURE OF THE STATE OF IDAHO             ||||
 Fifty-seventh Legislature                 First Regular Session - 2003
                                                                        
                                                                        
                              IN THE HOUSE OF REPRESENTATIVES
                                                                        
                                     HOUSE BILL NO. 237
                                                                        
                              BY HEALTH AND WELFARE COMMITTEE
                                                                        
  1                                        AN ACT
  2    RELATING TO CONTROLLED SUBSTANCES AND THE IDAHO BOARD  OF  PHARMACY;  AMENDING
  3        SECTION   37-2705,   IDAHO  CODE,  TO  EXPAND  THE  DESCRIPTION  OF  GAMMA
  4        HYDROXYBUTYRIC ACID PRODUCTS LISTED TO MATCH THE DESCRIPTION IN SCHEDULE I
  5        OF CONTROLLED SUBSTANCES UNDER FEDERAL LAW,  TO  ALLOW  SPECIFIC  PRODUCTS
  6        CONTAINING  GAMMA  HYDROXYBUTYRIC ACID TO BE PLACED IN OTHER SCHEDULES AND
  7        TO MAKE TECHNICAL CORRECTIONS; AMENDING SECTION 37-2709,  IDAHO  CODE,  TO
  8        ADD THE SUBSTANCE BUPRENORPHINE TO SCHEDULE III AND TO ADD TO SCHEDULE III
  9        ANY  DRUG  PRODUCT  CONTAINING  GAMMA  HYDROXYBUTYRIC  ACID, INCLUDING ITS
 10        SALTS, ISOMERS AND SALTS OF ISOMERS FOR WHICH AN APPLICATION  IS  APPROVED
 11        UNDER  SECTION  505  OF  THE FEDERAL FOOD, DRUG AND COSMETIC ACT; AMENDING
 12        SECTION 37-2713, IDAHO CODE, TO REMOVE THE  SUBSTANCE  BUPRENORPHINE  FROM
 13        SCHEDULE  V  AND  TO  MAKE  A  TECHNICAL  CORRECTION; AND AMENDING SECTION
 14        37-2732C, IDAHO CODE, TO INCLUDE THE SUBSTANCES LISTED IN  SUBSECTION  (e)
 15        OF  SECTION  37-2705,  IDAHO  CODE,  AND ANY DRUG PRODUCT CONTAINING GAMMA
 16        HYDROXYBUTYRIC ACID, INCLUDING ITS SALTS, ISOMERS AND SALTS OF ISOMERS FOR
 17        WHICH AN APPLICATION IS APPROVED UNDER SECTION 505 OF  THE  FEDERAL  FOOD,
 18        DRUG AND COSMETIC ACT UNDER THE PENALTY PROVISIONS FOR PERSONS BEING UNDER
 19        THE  INFLUENCE  OF A CONTROLLED SUBSTANCE AND BEING ON A PUBLIC ROADWAY OR
 20        CONVEYANCE.
                                                                        
 21    Be It Enacted by the Legislature of the State of Idaho:
                                                                        
 22        SECTION 1.  That Section 37-2705, Idaho Code, be, and the same  is  hereby
 23    amended to read as follows:
                                                                        
 24        37-2705.  SCHEDULE I. (a) The controlled substances listed in this section
 25    are included in schedule I.
 26        (b)  Any  of  the  following  opiates,  including  their  isomers, esters,
 27    ethers, salts, and salts of isomers, esters, and ethers,  unless  specifically
 28    excepted, whenever the existence of these isomers, esters, ethers and salts is
 29    possible within the specific chemical designation:
 30        (1)  Acetyl-alpha-methylfentanyl             (N-[1-(1-methyl-2-phenethyl)-
 31        4-piperidinyl]-N-phenylacetamide);
 32        (2)  Acetylmethadol;
 33        (3)  Allylprodine;
 34        (4)  Alphacetylmethadol  (except  levo-alphacetylmethadol  also  known  as
 35        levo-alpha-acetylmethadol, levomethadyl acetate or LAAM);
 36        (5)  Alphameprodine;
 37        (6)  Alphamethadol;
 38        (7)  Alpha-methylfentanyl;
 39        (8)  Alpha-methylthiofentanyl           (N-[1-methyl-2-(2-thienyl)ethyl-4-
 40        piperidinyl]-N-phenylpropanamide);
 41        (9)  Benzethidine;
 42        (10) Betacetylmethadol;
 43        (11) Beta-hydroxyfentanyl
                                                                        
                                           2
                                                                        
  1        (N-[1-(2-hydroxy-2-phenethyl)-4-piperidinyl]-N-phenylpropanamide);
  2        (12) Beta-hydroxy-3-methylfentanyl           (N-(1-(2-hydroxy-2-phenethyl)
  3        -3-methyl-4-piperidinyl)-N-phenylpropanamide);
  4        (13) Betameprodine;
  5        (14) Betamethadol;
  6        (15) Betaprodine;
  7        (16) Clonitazene;
  8        (17) Dextromoramide;
  9        (18) Diampromide;
 10        (19) Diethylthiambutene;
 11        (20) Difenoxin;
 12        (21) Dimenoxadol;
 13        (22) Dimepheptanol;
 14        (23) Dimethylthiambutene;
 15        (24) Dioxaphetyl butyrate;
 16        (25) Dipipanone;
 17        (26) Ethylmethylthiambutene;
 18        (27) Etonitazene;
 19        (28) Etoxeridine;
 20        (29) Furethidine;
 21        (30) Hydroxypethidine;
 22        (31) Ketobemidone;
 23        (32) Levomoramide;
 24        (33) Levophenacylmorphan;
 25        (34) 3-Methylfentanyl;
 26        (35) 3-methylthiofentanyl              (N-[(3-methyl-1-(2-thienyl)ethyl-4-
 27        piperidinyl]-N-phenylpropanamide);
 28        (36) Morpheridine;
 29        (37) MPPP (1-methyl-4-phenyl-4-propionoxypiperidine);
 30        (38) Noracymethadol;
 31        (39) Norlevorphanol;
 32        (40) Normethadone;
 33        (41) Norpipanone;
 34        (42) Para-fluorofentanyl         (N-(4-fluorophenyl)-N-[1-(2-phenethyl)-4-
 35        piperidinyl] propanamide);
 36        (43) PEPAP (1-(-2-phenethyl)-4-phenyl-4-acetoxypiperidine);
 37        (44) Phenadoxone;
 38        (45) Phenampromide;
 39        (46) Phenomorphan;
 40        (47) Phenoperidine;
 41        (48) Piritramide;
 42        (49) Proheptazine;
 43        (50) Properidine;
 44        (51) Propiram;
 45        (52) Racemoramide;
 46        (53) Thiofentanyl          (N-phenyl-N-[1-(2-thienyl)ethyl-4-piperidinyl]-
 47        propanamide);
 48        (54) Tilidine;
 49        (55) Trimeperidine.
 50        (c)  Any  of  the  following  opium  derivatives, their salts, isomers and
 51    salts of isomers, unless specifically  excepted,  whenever  the  existence  of
 52    these  salts,  isomers    and salts of isomers is possible within the specific
 53    chemical designation:
 54        (1)  Acetorphine;
 55        (2)  Acetyldihydrocodeine;
                                                                        
                                           3
                                                                        
  1        (3)  Benzylmorphine;
  2        (4)  Codeine methylbromide;
  3        (5)  Codeine-N-Oxide;
  4        (6)  Cyprenorphine;
  5        (7)  Desomorphine;
  6        (8)  Dihydromorphine;
  7        (9)  Drotebanol;
  8        (10) Etorphine (except hydrochloride salt);
  9        (11) Heroin;
 10        (12) Hydromorphinol;
 11        (13) Methyldesorphine;
 12        (14) Methyldihydromorphine;
 13        (15) Morphine methylbromide;
 14        (16) Morphine methylsulfonate;
 15        (17) Morphine-N-Oxide;
 16        (18) Myrophine;
 17        (19) Nicocodeine;
 18        (20) Nicomorphine;
 19        (21) Normorphine;
 20        (22) Pholcodine;
 21        (23) Thebacon.
 22        (d)  Hallucinogenic substances. Any material, compound, mixture or  prepa-
 23    ration which contains any quantity of the following hallucinogenic substances,
 24    their salts, isomers and salts of isomers, unless specifically excepted, when-
 25    ever  the  existence of these salts, isomers, and salts of isomers is possible
 26    within the specific chemical designation (for purposes of this paragraph only,
 27    the term "isomer" includes the optical, position and geometric isomers):
 28        (1)  4-bromo-2,5-dimethoxy amphetamine;
 29        (2)  2,5-dimethoxyamphetamine;
 30        (3)  4-bromo-2,5-dimethoxyphenethylamine   (some   other   names:   alpha-
 31        desmethyl DOB, 2C-B);
 32        (4)  2,5-dimethoxy-4-ethylamphetamine (another name: DOET);
 33        (5)  4-methoxyamphetamine (PMA);
 34        (6)  5-methoxy-3,4-methylenedioxy-amphetamine;
 35        (7)  4-methyl-2,5-dimethoxy-amphetamine (DOM, STP);
 36        (8)  3,4-methylenedioxy amphetamine;
 37        (9)  3,4-methylenedioxymethamphetamine (MDMA);
 38        (10) 3,4-methylenedioxy-N-ethylamphetamine (also known  as  N-ethyl-alpha-
 39        methyl-3,4 (methylenedioxy) phenethylamine, and N-ethyl MDA, MDE, MDEA);
 40        (11) N-hydroxy-3,4-methylenedioxyamphetamine  (also  known  as  N-hydroxy-
 41        alpha-methyl-3,4(methylenedioxy) phenethylamine, and N-hydroxy MDA);
 42        (12) 3,4,5-trimethoxy amphetamine;
 43        (13) Alpha-ethyltryptamine     (some     other     names:     etryptamine,
 44        3-(2-aminobutyl) indole);
 45        (14) Bufotenine;
 46        (15) Diethyltryptamine (DET);
 47        (16) Dimethyltryptamine (DMT);
 48        (17) Ibogaine;
 49        (18) Lysergic acid diethylamide;
 50        (19) Marihuana;
 51        (20) Mescaline;
 52        (21) Parahexyl;
 53        (22) Peyote;
 54        (23) N-ethyl-3-piperidyl benzilate;
 55        (24) N-methyl-3-piperidyl benzilate;
                                                                        
                                           4
                                                                        
  1        (25) Psilocybin;
  2        (26) Psilocyn;
  3        (27) Tetrahydrocannabinols.  Synthetic  equivalents of the substances con-
  4        tained in the plant, or in  the  resinous  extractives  of  Cannabis,  sp.
  5        and/or  synthetic  substances, derivatives, and their isomers with similar
  6        chemical structure and pharmacological activity such as the following:
  7            cis or trans tetrahydrocannabinol, and their optical isomers,  exclud-
  8        ing dronabinol in sesame oil and encapsulated in a soft gelatin capsule in
  9        a drug product approved by the U.S. Food and Drug Administration.
 10            cis or trans tetrahydrocannabinol, and their optical isomers.
 11            cis  or  trans  tetrahydrocannabinol,  and its optical isomers. (Since
 12        nomenclature of these substances is not internationally standardized, com-
 13        pounds of these structures, regardless of numerical designation of  atomic
 14        positions are covered.)
 15        (28) Ethylamine  analog  of phencyclidine (N-ethyl-1-phenylcyclohexylamine
 16        (1-phenylcyclohexyl)   ethylamine;   N-(1-phenylcyclohexyl)    ethylamine,
 17        cyclohexamine, PCE;
 18        (29) Pyrrolidine    analog    of    phencyclidine:   1-(phenylcyclohexy1l)
 19        -pyrrolidine, PCPy, PHP;
 20        (30) Thiophene             analog             of             phencyclidine
 21        1-[1-(2-thienyl)-cyclohexyl]-piperidine, 2-thienylanalog of phencyclidine,
 22        TPCP, TCP;
 23        (31) 1-[1-(2-thienyl) cyclohexyl] pyrrolidine another name: TCPy.
 24        (e)  Unless specifically excepted or unless listed  in  another  schedule,
 25    aAny material, compound, mixture or preparation which contains any quantity of
 26    the  following  substances  having  a depressant effect on the central nervous
 27    system, including its salts, isomers, and salts of isomers  wherever  whenever
 28    the  existence of such salts, isomers, and salts of isomers is possible within
 29    the specific chemical designation:
 30        (1)  Gamma hydroxybutyrate hydroxybutyric acid (some other  names  include
 31        GHB;   gamma-hydroxybutyrate,  4-hydroxybutyrate;  4-hyroxybutanoic  acid;
 32        sodium oxybate; sodium oxybutyrate);
 33        (2)  Flunitrazepam (also known as "R2", "Rohypnol");
 34        (3)  Mecloqualone;
 35        (4)  Methaqualone.
 36        (f)  Stimulants. Unless specifically excepted or unless listed in  another
 37    schedule,  any  material, compound, mixture, or preparation which contains any
 38    quantity of the following substances having a stimulant effect on the  central
 39    nervous system, including its salts, isomers, and salts of isomers:
 40        (1)  Aminorex         (some        other        names:        aminoxaphen,
 41        2-amino-5-phenyl-2-oxazoline, or 4,5-dihydro-5-phenyl-2-oxazolamine);
 42        (2)  Cathinone    (some     other     names:     alpha-aminopropiophenone,
 43        2-aminopropiophenone and norephedrone);
 44        (3)  Fenethylline;
 45        (4)  Methcathinone   (some  other  names:  2-(methyl-amino)-propiophenone,
 46        alpha-(methylamino)-propiophenone,  N-methylcathinone,   AL-464,   AL-422,
 47        AL-463 and UR1423);
 48        (5)  (t)cis-4-methylaminorex
 49        [(+/-)cis-4,5-dihydro-4-methyl-5-phenyl-2-oxazolamine];
 50        (6)  N-ethylamphetamine;
 51        (7)  N,N-dimethylamphetamine    (also   known   as:   N,N-alpha-trimethyl-
 52        benzeneethanamine).
 53        (g)  Temporary listing of substances subject to emergency scheduling.  Any
 54    material,  compound, mixture or preparation which contains any quantity of the
 55    following substances:
                                                                        
                                           5
                                                                        
  1        (1)  N-[1-benzyl-4-piperidyl]-N-phenylpropanamide  (benzylfentanyl),   its
  2        optical isomers, salts and salts of isomers.
  3        (2)  N-[1-(2-thienyl)methyl-4-piperidyl]-N-phenylpropanamide
  4        (thenylfentanyl), its optical isomers, salts and salts of isomers.
  5        (3)  4-methylaminorex      (also      known      as      2-amino-4-methyl-
  6        5-phenyl-2-oxazoline).
                                                                        
  7        SECTION  2.  That  Section 37-2709, Idaho Code, be, and the same is hereby
  8    amended to read as follows:
                                                                        
  9        37-2709.  SCHEDULE III. (a) Schedule III shall consist of  the  drugs  and
 10    other  substances,  by  whatever official name, common or usual name, chemical
 11    name, or brand name designated, listed in this section.
 12        (b)  Stimulants. Unless specifically excepted or unless listed in  another
 13    schedule,  any  material, compound, mixture, or preparation which contains any
 14    quantity of the following substances having a stimulant effect on the  central
 15    nervous  system, including its salts, isomers, (whether optical or geometric),
 16    and salts of such isomers whenever the existence of such salts,  isomers,  and
 17    salts of isomers is possible within the specific chemical designation:
 18        (1)  Those  compounds,  mixtures, or preparations in dosage unit form con-
 19        taining any stimulant substances listed in schedule  II  which  compounds,
 20        mixtures, or preparations were listed on August 25, 1971, as excepted com-
 21        pounds  under  C.F.R.  Sec. 308.32, and any other drug of the quantitative
 22        composition shown in that list for those drugs or which is the same except
 23        that it contains a lesser quantity of controlled substances.
 24        (2)  Benzphetamine;
 25        (3)  Chlorphentermine;
 26        (4)  Clortermine;
 27        (5)  Phendimetrazine.
 28        (c)  Depressants. Unless listed in another schedule,  any  material,  com-
 29    pound,  mixture,  or  preparation which contains any quantity of the following
 30    substances having a potential for abuse associated with a depressant effect on
 31    the central nervous system:
 32        (1)  Any compound, mixture or preparation containing:
 33             i.   Amobarbital;
 34             ii.  Secobarbital;
 35             iii. Pentobarbital or any salt thereof and  one  (1)  or  more  other
 36             active medicinal ingredients which are not listed in any schedule.
 37        (2)  Any suppository dosage form containing:
 38             i.   Amobarbital;
 39             ii.  Secobarbital;
 40             iii. Pentobarbital  or any salt of any of these drugs and approved by
 41             the Food and Drug Administration for marketing only as a suppository.
 42        (3)  Any  substance  which  contains  any  quantity  of  a  derivative  of
 43        barbituric acid or any salt thereof;
 44        (4)  Chlorhexadol;
 45        (5)  Any drug product containing gamma hydroxybutyric acid, including  its
 46        salts, isomers, and salts of isomers, for which an application is approved
 47        under section 505 of the federal food, drug, and cosmetic act;
 48        (6)  Ketamine, its salts, isomers, and salts of isomers - 7285. (Some other
 49        names for ketamine: (+  )-2-(2-chlorophenyl)-2-(methylamino)-cyclohexanone).
 50        (67)  Lysergic acid;
 51        (78)  Lysergic acid amide;
 52        (89)  Methyprylon;
 53        (910) Sulfondiethylmethane;
                                                                        
                                           6
                                                                        
  1        (101) Sulfonethylmethane;
  2        (112) Sulfonmethane;
  3        (123) Tiletamine and zolazepam or any salt thereof.
  4        (d)  Nalorphine.
  5        (e)  Narcotic drugs.
  6        (1)  Unless  specifically  excepted  or unless listed in another schedule,
  7        any material, compound, mixture, or preparation containing limited quanti-
  8        ties of any of the following narcotic drugs, or any salts thereof:
  9             (1i)    Not more than 1.8 grams of codeine, or any of its salts,  per
 10             100  milliliters or not more than 90 milligrams per dosage unit, with
 11             an equal or greater quantity of an isoquinoline alkaloid of opium;
 12             (2ii)   Not more than 1.8 grams of codeine, or any of its salts,  per
 13             100  milliliters or not more than 90 milligrams per dosage unit, with
 14             one (1) or more active, nonnarcotic ingredients in recognized  thera-
 15             peutic amounts;
 16             (3iii)  Not  more  than 300 milligrams of dihydrocodeinone, or any of
 17             its salts, per 100 milliliters or not more  than  15  milligrams  per
 18             dosage  unit,  with a fourfold or greater quantity of an isoquinoline
 19             alkaloid of opium;
 20             (4iv)   Not more than 300 milligrams of dihydrocodeinone, or  any  of
 21             its  salts,  per  100  milliliters or not more than 15 milligrams per
 22             dosage unit, with one (1) or more active, nonnarcotic ingredients  in
 23             recognized therapeutic amounts;
 24             (5v)    Not  more  than  1.8  grams  of dihydrocodeine, or any of its
 25             salts, per 100 milliliters or not more than 90 milligrams per  dosage
 26             unit,  with one (1) or more active, nonnarcotic ingredients in recog-
 27             nized therapeutic amounts;
 28             (6vi)   Not more than 300 milligrams of ethylmorphine, or any of  its
 29             salts,  per 100 milliliters or not more than 15 milligrams per dosage
 30             unit, with one (1) or  more  ingredients  in  recognized  therapeutic
 31             amounts;
 32             (7vii)  Not  more than 500 milligrams of opium per 100 milliliters or
 33             per 100 grams, or not more than 25 milligrams per dosage  unit,  with
 34             one  (1) or more active, nonnarcotic ingredients in recognized thera-
 35             peutic amounts;
 36             (8viii) Not more than 50 milligrams of morphine, or any of its salts,
 37             per 100 milliliters or per 100 grams with one  (1)  or  more  active,
 38             nonnarcotic ingredients in recognized therapeutic amounts.
 39        (2)  Any material, compound, mixture, or preparation containing any of the
 40        following narcotic drugs or their salts, as set forth below:
 41             (i)   Buprenorphine.
 42             (ii)  [Reserved].
 43        (f)  Anabolic  steroids  and  human  growth hormones. Any drug or hormonal
 44    substance, chemically and pharmacologically  related  to  testosterone  (other
 45    than  estrogens,  progestins  and corticosteroids) that promotes muscle growth
 46    including any salt, ester or isomer of a drug  or  substance  listed  in  this
 47    paragraph, if that salt, ester or isomer promotes muscle growth.
 48        (1)  Boldenone;
 49        (2)  Chlorotestosterone (4-chlortestosterone);
 50        (3)  Chorionic gonadotropin;
 51        (4)  Clostebol;
 52        (5)  Dehydrochlormethyltestosterone;
 53        (6)  Dihydrotestosterone (4-dihydrotestosterone);
 54        (7)  Drostanolone;
 55        (8)  Ethylestrenol;
                                                                        
                                           7
                                                                        
  1        (9)  Fluoxymesterone;
  2        (10) Formebulone;
  3        (11) Human growth hormones;
  4        (12) Mesterolone;
  5        (13) Methandienone;
  6        (14) Methandranone;
  7        (15) Methandriol;
  8        (16) Methandrostenolone;
  9        (17) Methenolone;
 10        (18) Methyltestosterone;
 11        (19) Mibolerone;
 12        (20) Nandrolone;
 13        (21) Norethandrolone;
 14        (22) Oxandrolone;
 15        (23) Oxymesterone;
 16        (24) Oxymetholone;
 17        (25) Stanolone;
 18        (26) Stanozolol;
 19        (27) Testolactone;
 20        (28) Testosterone;
 21        (29) Testosterone cypionate;
 22        (30) Testosterone enanthate;
 23        (31) Testosterone propionate;
 24        (32) Trenbolone.
 25        Anabolic  steroids  that are expressly intended for administration through
 26    implants to cattle or other nonhuman species, and that  are  approved  by  the
 27    federal  Food and Drug Administration for such use, shall not be classified as
 28    controlled substances under this act and shall not be governed by  its  provi-
 29    sions.
 30        In  addition to the penalties prescribed in article IV of the uniform con-
 31    trolled substances act, any person shall be guilty of a felony who prescribes,
 32    dispenses, supplies, sells,  delivers,  manufactures  or  possesses  with  the
 33    intent  to  prescribe, dispense, supply, sell, deliver or manufacture anabolic
 34    steroids or any other human growth hormone for purposes of  enhancing  perfor-
 35    mance  in  an  exercise,  sport  or  game or hormonal manipulation intended to
 36    increase muscle mass, strength or weight without a medical necessity as deter-
 37    mined by a physician.
 38        (g) Hallucinogenic substances.
 39        (1)  Dronabinol (synthetic) in sesame oil and encapsulated in a soft gela-
 40        tin capsule in the federal Food and Drug Administration approved product -
 41        7369.    (Some     other     names     for     dronabinol:     (6aR-trans)
 42        -6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo [b,d]pyran-1-ol
 43        or (-)-delta-9-(trans)-tetrahydrocannabinol).
 44        (h)  Other  substances.  Unless specifically excepted, or unless listed in
 45    another schedule, any material, compound, mixture, or preparation  which  con-
 46    tains any quantity of the following substance, including its salts:
 47        (1)  Butorphanol.
 48        (i)  The  board  may  except by rule any compound, mixture, or preparation
 49    containing any stimulant or depressant substance listed in subsections (b) and
 50    (c) of this section from the application of all or any part of this act if the
 51    compound, mixture, or preparation contains one (1) or  more  active  medicinal
 52    ingredients not having a stimulant or depressant effect on the central nervous
 53    system,  and if the admixtures are included therein in combinations, quantity,
 54    proportion, or concentration that vitiate the potential for abuse of the  sub-
 55    stances  which  have  a  stimulant or depressant effect on the central nervous
                                                                        
                                           8
                                                                        
  1    system.
                                                                        
  2        SECTION 3.  That Section 37-2713, Idaho Code, be, and the same  is  hereby
  3    amended to read as follows:
                                                                        
  4        37-2713.  SCHEDULE  V. (a) Schedule V shall consist of the drugs and other
  5    substances, by whatever official name, common or usual name, chemical name, or
  6    brand name designated, listed in this section.
  7        (b)  Narcotic drugs. Unless specifically  excepted  or  unless  listed  in
  8    another  schedule,  any material, compound, mixture, or preparation containing
  9    any of the following narcotic drugs and their salts, as set forth below:
 10        (1)  Buprenorphine.
 11        (c)  Narcotic drugs containing nonnarcotic active  medicinal  ingredients.
 12    Any  compound, mixture, or preparation containing any of the following limited
 13    quantities of narcotic drugs or salts thereof, which shall include one (1)  or
 14    more nonnarcotic active medicinal ingredients in sufficient proportion to con-
 15    fer  upon  the compound, mixture, or preparation, valuable medicinal qualities
 16    other than those possessed by the narcotic drug alone:
 17        (1)  Not more than 200 milligrams of codeine per 100  milliliters  or  per
 18        100 grams;
 19        (2)  Not  more  than 100 milligrams of dihydrocodeine  per 100 milliliters
 20        or per 100 grams;
 21        (3)  Not more than 100 milligrams of ethylmorphine  per 100 milliliters or
 22        per 100 grams;
 23        (4)  Not more than 2.5 milligrams of diphenoxylate and not  less  than  25
 24        micrograms of atropine sulfate per dosage unit;
 25        (5)  Not  more than 100 milligrams of opium per 100 milliliters or per 100
 26        grams;
 27        (6)  Not  more  than  0.5  milligrams  difenoxin  and  not  less  than  25
 28        micrograms of atropine sulfate per dosage unit.
 29        (d)  Other substances. Unless specifically excepted or  unless  listed  in
 30    another  schedule,  any  material, compound, mixture or preparation which con-
 31    tains any quantity of the following substances, including its salts:
 32        (1)  Propylhexedrine (except as Benzedrex [TM] inhaler);
 33        (2)  Pyrovalerone.
                                                                        
 34        SECTION 4.  That Section 37-2732C, Idaho Code, be, and the same is  hereby
 35    amended to read as follows:
                                                                        
 36        37-2732C.  USING  OR BEING UNDER THE INFLUENCE -- PENALTIES. (a) Except as
 37    authorized in this chapter, it is unlawful for any person on a public roadway,
 38    on a public conveyance, on public property or on private property open to  the
 39    public, to use or be under the influence of any controlled substance specified
 40    in  subsection  (b),  (c), (d), (e) and (f) of section 37-2705, Idaho Code, or
 41    subsection (b), (c) and (d) of section  37-2707,  Idaho  Code,  or  subsection
 42    (c)(5)  of  section  37-2709,  Idaho  Code, or any narcotic drug classified in
 43    schedule III, IV or V, except when administered by or under the direction of a
 44    person licensed by the state to dispense, prescribe, or administer  controlled
 45    substances.   It  shall  be  the  burden  of the defense to show that it comes
 46    within this exception.
 47        (b)  Any person convicted of violating the provisions of subsection (a) of
 48    this section is guilty of a misdemeanor and is punishable by imprisonment in a
 49    county jail for not more than six (6) months, or by a fine not  exceeding  one
 50    thousand dollars ($1,000) or by both.
 51        (c)  Any  person who is convicted of violating subsection (a) of this sec-
                                                                        
                                           9
                                                                        
  1    tion, when the offense occurred within five (5) years  of  that  person  being
  2    convicted  of  two  (2) or more separate violations of that subsection and who
  3    refuses to complete a licensed drug  rehabilitation  program  offered  by  the
  4    court  pursuant  to  subsection  (d)  shall be punished by imprisonment in the
  5    county jail for a mandatory minimum period of time of not less than  one  hun-
  6    dred  twenty (120) days, nor more than one (1) year.  The court may not reduce
  7    the mandatory minimum period of incarceration provided in this subsection.
  8        (d)  The court may, when it would be in the interest  of  justice,  permit
  9    any person convicted of a violation of subsection (a) of this section, punish-
 10    able  under subsection (b) or (c) of this section, to complete a licensed drug
 11    rehabilitation program in lieu of part or  all  of  the  imprisonment  in  the
 12    county jail.  As a condition of sentencing, the court may require the offender
 13    to pay all or a portion of the drug rehabilitation program.  In order to alle-
 14    viate  jail overcrowding and to provide recidivist offenders with a reasonable
 15    opportunity to seek rehabilitation pursuant to this subsection,  counties  are
 16    encouraged  to include provisions to augment licensed drug rehabilitation pro-
 17    grams in their substance abuse proposals and  applications  submitted  to  the
 18    state for federal and state drug abuse funds.
 19        (e)  Notwithstanding  subsection  (a),  (b) or (c) of this section, or any
 20    other  provision of law to the contrary, any person who  is  unlawfully  under
 21    the   influence   of   cocaine,  cocaine  base,  methamphetamine,  heroin,  or
 22    phencyclidine while in the immediate personal possession of a loaded, operable
 23    firearm is guilty of a public offense and is punishable by imprisonment in the
 24    county jail or the state prison for not more than one (1) year.   As  used  in
 25    this  subsection,  "immediate possession" includes, but is not limited to, the
 26    interior passenger compartment of a motor vehicle.
 27        (f)  Every person who violates subsection (e) of this section  is  punish-
 28    able  upon  the  second  and each subsequent conviction by imprisonment in the
 29    state prison for a period of time not in excess of four (4) years.
 30        (g)  In addition to any fine assessed under this section and notwithstand-
 31    ing the provisions of section 19-4705, Idaho Code, the court may, upon convic-
 32    tion, assess an additional cost to the defendant in the way of restitution, an
 33    amount not to exceed two hundred dollars  ($200) to the arresting and/or pros-
 34    ecuting agency or entity. These funds shall be  remitted  to  the  appropriate
 35    fund to offset the expense of toxicology testing.

Statement of Purpose / Fiscal Impact


                      STATEMENT OF PURPOSE
                                
                           RS 12904C1
                                
                                   This bill is necessary adjust the schedule of controlled
    substances in Idaho to match schedule adjustments by the
    federal Drug Enforcement Administration.  The proposed
    legislation moves the substance Buprenorphine from Schedule V
    (Idaho Code  37-2713(b)(1)) to Schedule III, revises Schedule
    I to allow specific products containing gamma hydroxybutyric
    acid to be placed in other schedules, adds to Schedule III any
    drug product containing gamma hydroxybutyric acid, including
    its salts, isomers, and salts of isomers, for which an
    application is approved under Section 505 of the Federal Food,
    Drug, and Cosmetic Act, and provides for penalties for using
    or being under the influence of any drug product containing
    gamma hydroxybutyric acid, including its salts, isomers, and
    salts of isomers, including unauthorized use of such a product
    for which an application is approved under Section 505 of the
    Federal Food, Drug, and Cosmetic Act.
    
    
    
    
    
    
    
    
    
    
    
                          FISCAL IMPACT
                                   
    There is no fiscal impact.
    
    
    
    
    
    
    CONTACT
    Name: R. K. "Mick" Markuson, Director 
    Agency: Idaho Board of Pharmacy
    Phone: (208) 334-2356
    
    
    
    
    
    
    Statement of Purpose/Fiscal Impact                H 23