[Code of Federal Regulations]
[Title 21, Volume 9]
[Revised as of April 1, 2007]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR1308.13]

[Page 96-98]
 
                         TITLE 21-FOOD AND DRUGS
 
   CHAPTER II--DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE
 
PART 1308_SCHEDULES OF CONTROLLED SUBSTANCES--Table of Contents
 
Sec. 1308.13  Schedule III.

    (a) Schedule III shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section. Each drug or substance has been 
assigned the DEA Controlled Substances Code Number set forth opposite 
it.
    (b) Stimulants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a stimulant 
effect on the central nervous sxstem, including its salts, isomers 
(whether optical, position, or geometric), and salts of such isomers 
whenever the existence of such salts, isomers, and salts of isomers is 
possible within the specific chemical designation:

(1) Those compounds, mixtures, or preparations in dosage unit       1405
 form containing any stimulant substances listed in schedule II
 which compounds, mixtures, or preparations were listed on August
 25, 1971, as excepted compounds under Sec. 1308.32, and any
 other drug of the quantitative composition shown in that list
 for those drugs or which is the same except that it contains a
 lesser quantity of controlled substances........................
(2) Benzphetamine................................................   1228

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(3) Chlorphentermine.............................................   1645
(4) Clortermine..................................................   1647
(5) Phendimetrazine..............................................   1615


    (c) Depressants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a depressant 
effect on the central nervous system:

(1) Any compound, mixture or preparation containing:
    (i) Amobarbital..............................................   2126
    (ii) Secobarbital............................................   2316
    (iii) Pentobarbital..........................................   2271
  or any salt thereof and one or more other active medicinal
   ingredients which are not listed in any schedule.
(2) Any suppository dosage form containing:
    (i) Amobarbital..............................................   2126
    (ii) Secobarbital............................................   2316
    (iii) Pentobarbital..........................................   2271
  or any salt of any of these drugs and approved by the Food and
   Drug Administration for marketing only as a suppository.
(3) Any substance which contains any quantity of a derivative of    2100
 barbituric acid or any salt thereof.............................
(4) Chlorhexadol.................................................   2510
(5) Embutramide..................................................   2020
(6) Any drug product containing gamma hydroxybutyric acid,          2012
 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..........................................
(7) Ketamine, its salts, isomers, and salts of isomers...........   7285
  [Some other names for ketamine: ()-2-(2-
   chlorophenyl)-2-(methylamino)-cyclohexanone]
(8) Lysergic acid................................................   7300
(9) Lysergic acid amide..........................................   7310
(10) Methyprylon.................................................   2575
(11) Sulfondiethylmethane........................................   2600
(12) Sulfonethylmethane..........................................   2605
(13) Sulfonmethane...............................................   2610
(14) Tiletamine and zolazepam or any salt thereof................   7295
  Some trade or other names for a tiletamine-zolazepam
   combination product:
    Telazol......................................................
  Some trade or other names for tiletamine:
    2-(ethylamino)-2-(2-thienyl)-cyclohexanone...................
  Some trade or other names for zolazepam:
    4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-[3,4-
     e] [1,4]-diazepin-7(1H)-one, flupyrazapon...................


    (d) Nalorphine 9400.
    (e) Narcotic drugs. Unless specifically excepted or unless listed in 
another schedule:

(1) Any material, compound, mixture, or preparation containing
 any of the following narcotic drugs, or their salts calculated
 as the free anhydrous base or alkaloid, in limited quantities as
 set forth below:
    (i) Not more than 1.8 grams of codeine per 100 milliliters or   9803
     not more than 90 milligrams per dosage unit, with an equal
     or greater quantity of an isoquinoline alkaloid of opium....
    (ii) Not more than 1.8 grams of codeine per 100 milliliters     9804
     or not more than 90 milligrams per dosage unit, with one or
     more active, nonnarcotic ingredients in recognized
     therapeutic amounts.........................................
    (iii) Not more than 300 milligrams of dihydrocodeinone          9805
     (hydrocodone) per 100 milliliters or not more than 15
     milligrams per dosage unit, with a fourfold or greater
     quantity of an isoquinoline alkaloid of opium...............
    (iv) Not more than 300 milligrams of dihydrocodeinone           9806
     (hydrocodone) per 100 milliliters or not more than 15
     milligrams per dosage unit, with one or more active
     nonnarcotic ingredients in recognized therapeutic amounts...
    (v) Not more than 1.8 grams of dihydrocodeine per 100           9807
     milliliters or not more than 90 milligrams per dosage unit,
     with one or more active nonnarcotic ingredients in
     recognized therapeutic amounts..............................
    (vi) Not more than 300 milligrams of ethylmorphine per 100      9808
     milliliters or not more than 15 milligrams per dosage unit,
     with one or more active, nonnarcotic ingredients in
     recognized therapeutic amounts..............................
    (vii) Not more than 500 milligrams of opium per 100             9809
     milliliters or per 100 grams or not more than 25 milligrams
     per dosage unit, with one or more active, nonnarcotic
     ingredients in recognized therapeutic amounts...............
    (viii) Not more than 50 milligrams of morphine per 100          9810
     milliliters or per 100 grams, with one or more active,
     nonnarcotic ingredients in recognized therapeutic amounts...
 (2) Any material, compound, mixture, or preparation containing
 any of the following narcotic drugs or their salts, as set forth
 below:
    (i) Buprenorphine............................................   9064
    (ii) [Reserved]..............................................


    (f) Anabolic Steroids. Unless specifically excepted or unless listed 
in another schedule, any material, compound, mixture or preparation 
containing any quantity of the following substances, including its 
salts, esters and ethers:
    (1) Anabolic steroids (see Sec. 1300.01 of this chapter)--4000
    (2) [Reserved]

    (g) Hallucinogenic substances. (1) Dronabinol (synthetic) in sesame 
oil and encapsulated in a soft gelatin capsule in a U.S. Food and Drug 
Administration approved product--7369.

[Some other names for dronabinol: (6aR-trans)-6a,7,8,10a-tetrahydro-
6,6,9-trimethyl-3-pentyl-6H-dibenzo [b,d]pyran-1-ol] or (-)-delta-9-
(trans)-tetrahydrocannabinol]


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    (2) [Reserved]

[39 FR 22142, June 20, 1974, as amended at 41 FR 43401, Oct. 1, 1976; 43 
FR 3359, Jan. 25, 1978; 44 FR 40888, July 13, 1979; 46 FR 52334, Oct. 
27, 1981; 51 FR 5320, Feb. 13, 1986; 52 FR 2222, Jan. 21, 1987; 52 FR 
5952, Feb. 27, 1987; 56 FR 5754, Feb. 13, 1991; 56 FR 11932, Mar. 21, 
1991; 62 FR 13968, Mar. 24, 1997; 64 FR 35930, July 2, 1999; 64 FR 
37675, July 13, 1999; 65 FR 13238, Mar. 13, 2000; 65 FR 17440, Apr. 3, 
2000; 67 FR 62370, Oct. 7, 2002; 70 FR 74657, Dec. 16, 2005; 71 FR 
51116, Aug. 29, 2006]