§ 63-2-208. Schedule III.

The controlled substances listed in this section are included in Schedule III.

A.  Unless listed in another schedule, any material, compound, mixture, or preparation, which contains any quantity of the following substances or any other substance having a potential for abuse associated with a stimulant or depressant effect on the central nervous system:

1.  Any drug product containing gamma-hydroxybutyric acid, including its salts, isomers, and salts of isomers, for which an application has been approved under Section 505 of the Federal Food, Drug, and Cosmetic Act;

2.  Any material, compound, mixture, or preparation which contains any quantity of the following hormonal substances or steroids, including their salts, isomers, esters and salts of isomers and esters, when the existence of these salts, isomers, esters, and salts of isomers and esters is possible within the specific chemical designation:

a.Boldenone,

b.Chlorotestosterone,

c.Clostebol,

d.Dehydrochlormethyltestosterone,

e.Dihydrotestosterone,

f.Drostanolone,

g.Ethylestrenol,

h.Fluoxymesterone,

i.Formebolone,

j.Mesterolone,

k.Methandienone,

l.Methandranone,

m.Methandriol,

n.Methandrostenolone,

o.Methenolone,

p.Methyltestosterone, except as provided in subsection E of this section,

q.Mibolerone,

r.Nandrolone,

s.Norethandrolone,

t.Oxandrolone,

u.Oxymesterone,

v.Oxymetholone,

w.Stanolone,

x.Stanozolol,

y.Testolactone,

z.Testosterone, except as provided in subsection E of this section, and

aa.Trenbolone;

3.  Any substance which contains any quantity of a derivative of barbituric acid, or any salt of a derivative of barbituric acid;

4.  Benzephetamine and its salts;

5.  Buprenorphine;

6.  Butalbital/acetaminophen/caffeine;

7.  Chlorhexadol;

8.  Chlorphentermine and its salts;

9.  Clortermine;

10.  Glutethimide;

11.  Hydrocodone with another active ingredient;

12.  Ketamine, its salts, isomers, and salts of isomers;

13.  Lysergic acid;

14.  Lysergic acid amide;

15.  Mazindol;

16.  Methyprylon;

17.  Phendimetrazine;

18.  Phenylacetone (P2P);

19.  Sulfondiethylmethane;

20.  Sulfonethylmethane;

21.  Sulfonmethane;

22.  Tetrahydrocannibinols;

23.  1-Phenycyclohexylamine; or

24.  1-Piperidinocychexanecarbo nitrile (PCC).

Livestock implants as regulated by the Federal Food and Drug Administration shall be exempt.

B.  Nalorphine.

C.  Unless listed in another schedule, any material, compound, mixture, or preparation containing limited quantities of any of the following narcotic drugs, or any salts thereof:

1.  Not more than one and eight-tenths (1.8) grams of codeine or any of its salts, per one hundred (100) milliliters or not more than ninety (90) milligrams per dosage unit, with an equal or greater quantity of an isoquinoline alkaloid of opium;

2.  Not more than one and eight-tenths (1.8) grams of codeine or any of its salts, per one hundred (100) milliliters or not more than ninety (90) milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;

3.  Not more than one and eight-tenths (1.8) grams of dihydrocodeine or any of its salts, per one hundred (100) milliliters or not more than ninety (90) milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;

4.  Not more than three hundred (300) milligrams of ethylmorphine or any of its salts, per one hundred (100) milliliters or not more than fifteen (15) milligrams per dosage unit, with one or more ingredients in recognized therapeutic amounts;

5.  Not more than five hundred (500) milligrams of opium per one hundred (100) milliliters or per one hundred (100) grams, or not more than twenty-five (25) milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts; or

6.  Not more than fifty (50) milligrams of morphine or any of its salts, per one hundred (100) milliliters or per one hundred (100) grams with one or more active, nonnarcotic ingredients in recognized therapeutic amounts.

D.  The Board of Pharmacy may except by rule any compound, mixture, or preparation containing any stimulant or depressant substance listed in subsections A and B of this section from the application of all or any part of the Uniform Controlled Dangerous Substances Act if the compound, mixture, or preparation contains one or more active medicinal ingredients not having a stimulant or depressant effect on the central nervous system, and if the admixtures are included therein in combinations, quantity, proportion, or concentration that vitiate the potential for abuse of the substances which have a stimulant or depressant effect on the central nervous system.

E.  The following hormonal substances or steroids are exempt from classification as Schedule III controlled dangerous substances:

1.  Estratest, containing 1.25 mg esterified estrogens and 2.5 mg methyltestosterone;

2.  Estratest HS, containing 0.625 mg esterified estrogens and 1.25 mg methyltestosterone;

3.  Premarin with Methyltestosterone, containing 1.25 mg conjugated estrogens and 10.0 mg methyltestosterone;

4.  Premarin with Methyltestosterone, containing 0.625 mg conjugated estrogens and 5.0 mg methyltestosterone;

5.  Testosterone Cypionate - Estrodiol Cypionate injection, containing 50 mg/ml Testosterone Cypionate; and

6.  Testosterone Enanthate - Estradiol Valerate injection, containing 90 mg/ml Testosterone Enanthate and 4 mg/ml Estradiol Valerate.

Added by Laws 1971, c. 119, § 2-208, operative Sept. 1, 1971.  Amended by Laws 1972, c. 229, § 3, emerg. eff. April 7, 1972; Laws 1976, c. 291, § 3, emerg. eff. June 17, 1976; Laws 1984, c. 127, § 3, eff. Nov. 1, 1984; Laws 1991, c. 306, § 1, emerg. eff. June 4, 1991; Laws 1993, c. 22, § 1, emerg. eff. March 29, 1993; Laws 1995, c. 54, § 3, eff. July 1, 1995; Laws 2001, c. 373, § 3, eff. July 1, 2001; Laws 2005, c. 283, § 3, eff. Nov. 1, 2005; Laws 2011, c. 239, § 4, eff. Nov. 1, 2011; Laws 2012, c. 80, § 3, eff. Nov. 1, 2012.