EXPEDITED RULES
(Board of Pharmacy)
Title of Rule: WAC 246-887-160 Schedule III.
Purpose: The purpose of this rule is to identify those drugs that have been designated as Schedule III controlled substances.
Statutory Authority for Adoption: RCW 69.50.201 and 18.64.005(7).
Statute Being Implemented: RCW 60.50.201 [69.50.201].
Summary: The proposed amendment will correct an error in the rule by removing Dehydroepiandrosterone (DHEA) from the listing of drugs in Schedule III of the regulations implementing the Uniform Controlled Substances Act.
Reasons Supporting Proposal: Amending the rule will correct an error and align the rule with federal rules.
Name of Agency Personnel Responsible for Drafting and Implementation: Lisa Salmi, 1300 Quince Street S.E., Olympia, WA 98504-7863, (360) 236-4828; and Enforcement: Donald Williams, 1300 S.E. Quince Street S.E., Olympia, WA 98504-7863.
Name of Proponent: Department of Health, Washington State Board of Pharmacy, 1300 S.E. Quince Street, P.O. Box 47863, Olympia, WA 98504-7863, governmental.
Rule is not necessitated by federal law, federal or state court decision.
Explanation of Rule, its Purpose, and Anticipated Effects: This rule lists drugs that have been designated as Schedule III controlled substances. The proposed amendment will remove dehydroepiandrosterone from this listing. Dehydroepiandrosterone was erroneously listed as a Schedule III controlled Substance. The proposed amendment will correct this error.
Proposal Changes the Following Existing Rules: Removes
Dehydroepiandrosterone from the listing of Schedule III
controlled substances.
THIS RULE IS BEING PROPOSED UNDER AN EXPEDITED RULE-MAKING PROCESS THAT WILL ELIMINATE THE NEED FOR THE AGENCY TO HOLD PUBLIC HEARINGS, PREPARE A SMALL BUSINESS ECONOMIC IMPACT STATEMENT, OR PROVIDE RESPONSES TO THE CRITERIA FOR A SIGNIFICANT LEGISLATIVE RULE. IF YOU OBJECT TO THE USE OF THE EXPEDITED RULE-MAKING PROCESS, YOU MUST EXPRESS YOUR OBJECTIONS IN WRITING AND THEY MUST BE SENT TO Lisa Salmi, Department of Health, Washington State Board of Pharmacy, P.O. Box 47863, Olympia, WA 98504-7863 , AND RECEIVED BY August 20, 2002.
April 15, 2002
D. H. Williams
Executive Director
OTS-5548.1
AMENDATORY SECTION(Amending WSR 00-10-113, filed 5/3/00)
WAC 246-887-160
Schedule III.
The board finds that the
following substances have a potential for abuse less than the
substances listed in Schedules I and II, and have currently
accepted medical use in treatment in the United States and that
the abuse of the substances may lead to moderate or low physical
dependency or high psychological dependency. The board,
therefore, places each of the following substances in Schedule
III.
(a) The drugs and other substances listed in this section, by whatever official name, common or usual name, chemical name, or brand name designated, are included in Schedule III.
(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 system, 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 form containing any stimulant substances listed in Schedule II which compounds, mixtures, or preparations are referred to as excepted compounds in Schedule III as published in 21 CFR 1308.13 (b)(1) as of April 1, 1984, 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;
(3) Chlorphentermine;
(4) Clortermine;
(5) Phendimetrazine.
(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;
(ii) Secobarbital;
(iii) Pentobarbital;
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;
(ii) Secobarbital;
(iii) Pentobarbital;
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 barbituric acid, or any salt of a derivative of barbituric acid;
(4) Chlorhexadol;
(5) Ketamine, its salts, isomers, and salts of isomers -- some other names for ketamine: (<plus-minus>)-2-(2- chlorophenyl)-2-(methylamino)-cyclohexanone;
(6) Lysergic acid;
(7) Lysergic acid amide;
(8) Methyprylon;
(9) Sulfondiethylmethane;
(10) Sulfonethylmethane;
(11) Sulfonmethane;
(12) Tiletamine and zolazepam or any salt thereof -- 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.
(e) Anabolic steroids. The term "anabolic steroid" means any drug or hormonal substance, chemically and pharmacologically related to testosterone (other than estrogens, progestins, and corticosteroids) that promotes muscle growth, and includes:
(1) Boldenone;
(2) Chlorotestosterone;
(3) Clostebol;
(4) Dehydrochlormethyltestosterone;
(5) ((Dehydroepiandrosterone;
(6))) Dihydrotestosterone;
(((7))) (6) Drostanolone;
(((8))) (7) Ethylestrenol;
(((9))) (8) Fluoxymesterone;
(((10))) (9) Formebulone (Formebolone);
(((11))) (10) Mesterolone;
(((12))) (11) Methandienone;
(((13))) (12) Methandranone;
(((14))) (13) Methandriol;
(((15))) (14) Methandrostenolone;
(((16))) (15) Methenolone;
(((17))) (16) Methyltestosterone;
(((18))) (17) Mibolerone;
(((19))) (18) Nandrolone;
(((20))) (19) Norethandrolone;
(((21))) (20) Oxandrolone;
(((22))) (21) Oxymesterone;
(((23))) (22) Oxymetholone;
(((24))) (23) Stanolone;
(((25))) (24) Stanozolol;
(((26))) (25) Testolactone;
(((27))) (26) Testosterone;
(((28))) (27) Trenbolone; and
(((29))) (28) Any salt, ester, or isomer of a drug or
substance described or listed in this paragraph, if that salt,
ester, or isomer promotes muscle growth. Except such term does
not include an anabolic steroid which is expressly intended for
administration through implants to cattle or other nonhuman
species and which has been approved by the secretary of health
and human services for such administration. If any person
prescribes, dispenses, or distributes such steroid for human use
such person shall be considered to have prescribed, dispensed, or
distributed an anabolic steroid within the meaning of this
paragraph.
The following are implants or pellets which are exempt:
Ingredients | Trade Name | Company |
Testosterone Propionate, Oestradiol Benzoate | F-TO | Animal Health Div. Upjohn International Kalamazoo, MI |
Trenbolone Acetate | Finaplix-H | Hoechst-Roussel
Agri-Vet Co., Somerville, NJ |
Trenbolone Acetate | Finaplix-S | Hoechst-Roussel
Agri-Vet Co., Somerville, NJ |
Testosterone Propionate, Estradiol Benzoate |
Heifer-oid | Anchor Division Boehringer Ingelheim St. Joseph, MO |
Testosterone Propionate, Estradiol Benzoate |
Heifer-oid | Bio-Ceutic Division
Boehringer Ingelheim St. Joseph, MO |
Testosterone Propionate, Estradiol Benzoate |
Heifer-oid | Ivy Laboratories, Inc. Overland Park, KS |
Testosterone Propionate, Estradiol Benzoate |
Implus | The Upjohn Co. Kalamazoo, MI |
Trenbolone Acetate, Estradiol |
Revalor-s | Hoechst-Roussel
Agri-Vet Co., Somerville, NJ |
Testosterone Propionate, Estradiol Benzoate |
Synovex H | Syntex Laboratories Palo Alto, CA |
(f) The following anabolic steroid products containing compounds, mixtures, or preparations are exempt from the recordkeeping, refill restrictions, and other Controlled Substances Act requirements:
Ingredients | Trade Name | Company |
Testosterone enanthate
90 mg/ml Estradiol valerate 4 mg/ml |
Androgyn L.A. | Forest
Pharmaceuticals St. Louis, MO |
Testosterone enanthate
90 mg/ml Estradiol valerate 4 mg/ml |
Andro-Estro 90-4 | Rugby Laboratories Rockville Centre, NY |
Testosterone cypionate
50 mg/ml Estradiol cypionate 2 mg/ml |
depANDROGYN | Forest
Pharmaceuticals St. Louis, MO |
Testosterone cypionate
50 mg/ml Estradiol cypionate 2 mg/ml |
DEPO-T.E. | Quality Research
Laboratories Carmel, IN |
Testosterone cypionate
50 mg/ml Estradiol cypionate 2 mg/ml |
depTESTROGEN | Martica
Pharmaceuticals Phoenix, AZ |
Testosterone enanthate
90 mg/ml Estradiol valerate 4 mg/ml |
Duomone | Wintec
Pharmaceutical Pacific, MO |
Testosterone cypionate
50 mg/ml Estradiol cypionate 2 mg/ml |
DURATESTRIN | W.E. Hauck Alpharetta, GA |
Testosterone cypionate
50 mg/ml Esterified cypionate 2 mg/ml |
DUO-SPAN II | Primedics
Laboratories Gardena, CA |
Esterified estrogens 1.25 mg. Methyltestosterone 2.5 mg. |
Estratest | Solvay
Pharmaceuticals Marietta, GA |
Esterified estrogens 0.525 mg. Methyltestosterone 1.25 mg. |
Estratest HS | Solvay
Pharmaceuticals Marietta, GA |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
PAN ESTRA TEST | Pan American Labs Covington, LA |
Conjugated estrogens 1.25 mg. Methyltestosterone 10 mg. |
Premarin with Methyltestosterone | Ayerst Labs, Inc. New York, NY |
Conjugated estrogens 0.625 mg. Methyltestosterone 5 mg. |
Premarin with Methyltestosterone | Ayerst Labs, Inc. New York, NY |
Testosterone propionate 25 mg Estradiol benzoate 2.5 mg |
Synovex H
Pellets in process |
Syntex Animal Health Palo Alto, CA |
Testosterone propionate 10 parts Estradiol benzoate 1 part |
Synovex H
Pellets in process, granulation |
Syntex Animal Health Palo Alto, CA |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testagen | Clint Pharmaceutical Nashville, TN |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
TEST-ESTRO Cypionates | Rugby Laboratories Rockville Centre, NY |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testosterone Cyp 50 Estradiol Cyp 2 | I.D.E.-Interstate Amityville, NY |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testosterone Cypionate-Estradiol Cypionate Injection | Best Generics No. Miami Beach, FL |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testosterone Cypionate-Estradiol Cypionate Injection | Goldline Labs Ft. Lauderdale FL |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testosterone Cypionate-Estradiol Cypionate Injection | Schein
Pharmaceuticals Port Washington, NY |
Testosterone cypionate 50 mg/ml Estradiol cypionate 2 mg/ml |
Testosterone Cypionate-Estradiol Cypionate Injection | Steris Labs, Inc. Phoenix, AZ |
Testosterone enanthate 90 mg/ml Estradiol valerate 4 mg/ml |
Testosterone Enanth-ate-Estradiol Valer-ate Injection | Goldline Labs Ft. Lauderdale FL |
Testosterone enanthate 90 mg/ml Estradiol valerate 4 mg/ml |
Testosterone Enanthate-Estradiol Valerate Injection | Schein
Pharmaceuticals Port Washington, NY |
Testosterone enanthate 90 mg/ml Estradiol valerate 4 mg/ml |
Testosterone Enanthate-Estradiol Valerate Injection | Steris Labs, Inc. Phoenix, AZ |
(1) Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with an equal or greater quantity of an isoquinoline alkaloid of opium;
(2) Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;
(3) Not more than 300 milligrams of dihydrocodeinone per 100 milliliters or not more than 15 milligrams per dosage unit, with a fourfold or greater quantity of an isoquinoline alkaloid of opium;
(4) Not more than 300 milligrams of dihydrocodeinone per 100 milliliters or not more than 15 milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;
(5) Not more than 1.8 grams of dihydrocodeine per 100 milliliters or not more than 90 milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;
(6) Not more than 300 milligrams of ethylmorphine per 100 milliliters or not more than 15 milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;
(7) Not more than 500 milligrams of opium per 100 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;
(8) Not more than 50 milligrams of morphine per 100 milliliters or per 100 grams with one or more active, nonnarcotic ingredients in recognized therapeutic amounts.
(h) Hallucinogenic substances.
(1) Dronabinol (synthetic) in sesame oil and encapsulated in a soft gelatin capsule in a United States Food and Drug Administration approved product. (Some other names for dronabinol [6aR-trans]-6a,7,8, 10a-tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d] pyran-i-ol, or (-)-delta-9-(trans)-tetrahydrocannabinol.)
[00-10-113, § 246-887-160, filed 5/3/00. 00-01-075, § 246-887-160, filed 12/13/99. Statutory Authority: RCW 18.64.005. 96-01-032, § 246-887-160, filed 12/12/95, effective 1/12/96; 94-08-098, § 246-887-160, filed 4/6/94, effective 5/7/94. Statutory Authority: RCW 18.64.005. 93-14-038 (Order 376B), § 246-887-160, filed 6/29/93, effective 7/30/93; 93-06-093 (Order 343B), § 246-887-160, filed 3/3/93, effective 4/3/93; 92-04-029 (Order 239B), § 246-887-160, filed 1/28/92, effective 2/29/92. Statutory Authority: RCW 18.64.005 and chapter 18.64A RCW. 91-18-057 (Order 191B), recodified as § 246-887-160, filed 8/30/91, effective 9/30/91. Statutory Authority: RCW 69.50.201. 89-17-023 (Order 226), § 360-36-430, filed 8/8/89, effective 9/8/89. Statutory Authority: RCW 69.50.201, 69.50.203, 69.50.205, 69.50.207, 69.50.209 and 69.50.211. 84-22-062 (Order 190), § 360-36-430, filed 11/7/84.]
Reviser's note: The brackets and enclosed material in the text of the above section occurred in the copy filed by the agency and appear in the Register pursuant to the requirements of RCW 34.08.040.