(1) if the proceeding is commenced by the filing of a petition, notice of the proposal made by the petition shall be published in general terms by the Secretary within thirty days after such filing, and the Secretary's order (required by paragraph (1) of section 371(e) of this title) acting upon such proposal shall, in the absence of prior referral (or request for referral) to an advisory committee, be issued within ninety days after the date of such filing, except that the Secretary may (prior to such ninetieth day), by written notice to the petitioner, extend such ninety-day period to such time (not more than one hundred and eighty days after the date of filing of the petition) as the Secretary deems necessary to enable him to study and investigate the petition; (2) any report, recommendations, underlying data, and reasons certified to the Secretary by an advisory committee appointed pursuant to subparagraph (D) of subsection (b) (5) of this section, shall be made a part of the record of any hearing if relevant and material, subject to the provisions of section 1006(c) of Title 5. The advisory committee shall designate a member to appear and testify at any such hearing with respect to the report and recommendations of such committee upon request of the Secretary, the petitioner, or the officer conducting the hearing, but this shall not preclude any other member of the advisory committee from appearing and testifying at such hearing; (3) the Secretary's order after public hearing (acting upon objections filed to an order made prior to hearing) shall be subject to the requirements of section 348(f) (2) of this title; and (4) the scope of judicial review of such order shall be in accordance with the fourth sentence of paragraph (2), and with the provisions of paragraph (3), of section 348 (g) of this title. (e) Fees. The admitting to listing and certification of color additives, in accordance with regulations prescribed under this chapter, shall be performed only upon payment of such fees, which shall be specified in such regulations, as may be necessary to provide, maintain, and equip an adequate service for such purposes. (f) Exemptions. The Secretary shall by regulations (issued without regard to subsection (d) of this section) provide for exempting from the requirements of this section any color additive or any specific type of use thereof, and any article of food, drug, or cosmetic bearing or containing such additive, intended solely for investigational use by qualified experts when in his opinion such exemption is consistent with the public health. (As amended July 12, 1960, Pub. L. 86-618, title I, § 103(b), 74 Stat. 399; Oct. 10, 1962, Pub. L. 87-781, title I, § 104(f) (2), 76 Stat 785.) AMENDMENTS 1962 Subsec. (b) (5) (B). Pub. L. 87-781 provided that clause (1) of this subparagraph shall not apply to a color additive in feed of animals raised for food production, if under the conditions of use specified in proposed labeling, and which conditions are reasonably certain to be fol lowed in practice, such additive will not adversely affect the animals and no residue will be found in any edible portion of such animal after slaughter or in any food from the living animal. 1960-Pub. L. 86-618 amended section generally. Section prior to the amendment by Pub. L. 86-618 provided: "The admitting to listing and certification of coal-tar colors, in accordance with regulations prescribed under this chapter, shall be performed only upon payment of such fees, which shall be specified in such regulations, as may be necessary to provide, maintain, and equip an adequate service for such purposes." EFFECTIVE DATE OF 1962 AMENDMENT; EXCEPTIONS Amendment of section by Pub. L. 87-781 effective on Oct. 10, 1962, see section 107 of Pub. L. 87-781, set out as a note under section 321 of this title. EFFECTIVE DATE OF 1960 AMENDMENT, TRANSITIONAL PROVISIONS, AND EFFECT ON OTHER LAWS Title II of Pub. L. 86-618 provided that: [DEFINITIONS.] "SEC. 201. As used in this title, the term 'basic Act' means the Federal Food, Drug, and Cosmetic Act; the term 'enactment date' means the date of enactment of this Act [July 12, 1960]; and other terms, insofar as also used in the basic Act (whether before or after enactment of this Act) shall have the same meaning as they have, or had when in effect, under the basic Act. "SEC. 202. [EFFECTIVE DATE.] This Act [amending this section and sections 321, 331, 333, 342, 343, 346, 351, 352, 361, 362, and 371 of this title and repealing sections 354 and 364 of this title] shall, subject to the provisions of section 203, take effect on the enactment date [July 12, 1960]. "SEC. 203. [PROVISIONAL LISTINGS OF COMMERCIALLY ESTABLISHED COLORS.] (a) (1) The purpose of this section is to make possible, on an interim basis for a reasonable period, through provisional listings, the use of commercially established color additives to the extent consistent with the public health, pending the completion of the scientific investigations needed as a basis for making determinations as to listing of such additives under the basic Act as amended by this Act. A provisional listing (including a deemed provisional listing) of a color additive under this section for any use shall, unless sooner terminated or expiring under the provisions of this section, expire (A) on the closing date (as defined in paragraph (2) of this subsection) or (B) on the effective date of a listing of such additive for such use under section 706 of the basic Act, this section whichever date first occurs. "(2) For the purposes of this section, the term 'closing date' means (A) the last day of the two and one-half year period beginning on the enactment date [July 12, 1960] or (B), with respect to a particular provisional listing (or deemed provisional listing) of a color additive or use thereof, such later closing date as the Secretary may from time to time establish pursuant to the authority of this paragraph. The Secretary may by regulation, upon application of an interested person or on his own initiative, from time to time postpone the original closing date with respect to a provisional listing (or deemed provisional listing) under this section of a specified color additive, or of a specified use or uses of such additive, for such period or periods as he finds necessary to carry out the purpose of this section, if in the Secretary's judgment such action is consistent with the objective of carrying to completion in good faith, as soon as reasonably practicable, the scientific investigations necessary for making a determination as to listing such additive, or such specified use or uses thereof, under section 706 of the basic Act [this section]. The Secretary may terminate a postponement of the closing date at any time if he finds that such postponement should not have been granted, or that by reason of a change in circumstances the basis for such postponement no longer exists, or that there has been a failure to comply with a requirement for submission of progress reports or with other conditions attached to such postponement. "(b) Subject to the other provisions of this section"(1) any color additive which, on the day preceding the enactment date [July 12, 1960], was listed and certifiable for any use or uses under section 406(b), 504, or 604 [section 346(b), 354, or 364 of this title], or under the third proviso of section 402(c) [section 342(c) of this title], of the basic Act, and of which a batch or batches had been certified for such use or uses prior to the enactment date [July 12, 1960], and "(2) any color additive which was commercially used or sold prior to the enactment date [July 12, 1960] for any use or uses in or on any food, drug, or cosmetic, and which either, (A), on the day preceding the enactment date [July 12, 1960], was not a material within the purview of any of the provisions of the basic Act enumerated in paragraph (1) of this subsection, or (B) is the color additive known as synthetic beta-carotene, shall, beginning on the enactment date [July 12, 1960], be deemed to be provisionally listed under this section as a color additive for such use or uses. "(c) Upon request of any person, the Secretary, by regulations issued under subsection (d), shall without delay, if on the basis of the data before him he deems such action consistent with the protection of the public health, provisionally list a material as a color additive for any use for which it was listed, and for which a batch or batches of such material had been certified, under section 406(b), 504, or 604 of the basic Act [section 346(b), 354, or 364 of this title] prior to the enactment date [July 12, 1960], although such color was no longer listed and certifiable for such use under such sections on the day preceding the enactment date. Such provisional listing shall take effect on the date of publication. "(d) (1) The Secretary shall, by regulations issued or amended from time to time under this section "(A) insofar as practicable promulgate and keep current a list or lists of the color additives, and of the particular uses thereof, which he finds are deemed provisionally listed under subsection (b), and the presence of a color additive on such a list with respect to a particular use shall, in any proceeding under the basic Act, be conclusive evidence that such provisional listing is in effect; "(B) provide for the provisional listing of the color additives and particular uses thereof specified in subsection (c); "(C) provide, with respect to particular uses for which color additives are or are deemed to be provisionally listed, such temporary tolerance limitations (including such limitations at zero level) and other conditions of use and labeling or packaging requirements, if any, as in his judgment are necessary to protect the public health pending listing under section 706 of the basic Act [this section]; "(D) provide for the certification of batches of such color additives (with or without diluents) for the uses for which they are so listed or deemed to be listed under this section, except that such an additive which is a color additive deemed provisionally listed under subsection (b) (2) of this section shall be deemed exempt from the requirement of such certification while not subject to a tolerance limitation; and "(E) provide for the termination of a provisional listing (or deemed provisional listing) of a color additive or particular use thereof forthwith whenever in his judgment such action is necessary to protect the public health. “(2)(A) Except as provided in subparagraph (C) of this paragraph, regulations under this section shall, from time to time, be issued, amended, or repealed by the Secretary without regard to the requirements of the basic Act [subsec. (e) of this section], but for the purposes of the application of section 706(e) of the basic Act (relating to fees) and of determining the availability of appropriations of fees (and of advance deposits to cover fees), proceedings, regulations, and certifications under this section shall be deemed to be proceedings, regulations, and certifications under such section 706 [this section]. Regulations providing for fees (and advance deposits to cover fees), which on the day preceding the enactment date [July 12, 1960] were in effect pursuant to section 706 of the basic Act [this section], shall be deemed to be regulations under such section 706 [this section] as amended by this Act, and appropriations of fees (and advance deposits) available for the purposes specified in such section 706 as in effect prior to the enactment date [July 12, 1960] shall be available for the purposes specified in such section 706 [this section] as so amended. "(B) If the Secretary, by regulation "(1) has terminated a provisional listing (or deemed provisional listing) of a color additive or particular use thereof pursuant to paragraph (1)(E) of this subsection; or "(11) has, pursuant to paragraph (1)(C) or paragraph (3) of this subsection, initially established or rendered more restrictive a tolerance limitation or other restriction or requirement with respect to a provisional listing (or deemed provisional listing) which listing had become effective prior to such action, any person adversely affected by such action may, prior to the expiration of the period specified in clause (A) of subsection (a)(2) of this section, file with the Secretary a petition for amendment of such regulation so as to revoke or modify such action of the Secretary, but the filing of such petition shall not operate to stay or suspend the effectiveness of such action. Such petition shall, in accordance with regulations, set forth the proposed amendment and shall contain data (or refer to data which are before the Secretary or of which he will take official notice), which show that the revocation or modification proposed is consistent with the protection of the public health. The Secretary shall, after publishing such proposal and affording all interested persons an opportunity to present their views thereon orally or in writing, act upon such proposal by published order. "(C) Any person adversely affected by an order entered under subparagraph (B) of this paragraph may, within thirty days after its publication, file objections thereto with the Secretary, specifying with particularity the provisions of the order deemed objectionable, stating reasonable grounds for such objections, and requesting a public hearing upon such objections. The Secretary shall hold a public hearing on such objections and shall, on the basis of the evidence adduced at such hearing, act on such objections by published order. Such order may reinstate a terminated provisional listing, or increase or dispense with a previously established temporary tolerance limitation, or make less restrictive any other limitation established by him under paragraph (1) or (3) of this subsection, only if in his judgment the evidence so adduced shows that such action will be consistent with the protection of the public health. An order entered under this subparagraph shall be subject to judicial review in accordance with section 701(f) of the basic Act [section 371 (f) of this title] except that the findings and order of the Secretary shall be sustained only if based upon a fair evaluation of the entire record at such hearing. No stay or suspension of such order shall be ordered by the court pending conclusion of such judicial review. "(D) On and after the enactment date [July 12, 1960], regulations, provisional listings, and certifications (or exemptions from certification) in effect under this section shall, for the purpose of determining whether an article is adulterated or misbranded within the meaning of the basic Act by reason of its being, bearing, or containing a color additive, have the same effect as would regulations, listings, and certifications (or exemptions from certification) under section 706 of the basic Act [this section]. A regulation, provisional listing or termination thereof, tolerance limitation, or certification or exemption therefrom, under this section shall not be the basis for any presumption or inference in any proceeding under section 706 (b) or (c) of the basic Act [subsec. (b) or (c) of this section]. "(3) For the purpose of enabling the Secretary to carry out his functions under paragraphs (1) (A) and (C) of this subsection with respect to color additives deemed provisionally listed, he shall, as soon as practicable after enactment of this Act [July 12, 1960], afford by public notice a reasonable opportunity to interested persons to submit data relevant thereto. If the data so submitted or otherwise before him do not, in his judgment, establish a reliable basis for including such a color additive or particular use or uses thereof in a list or lists promulgated under paragraph (1)(A), or for determining the prevailing level or levels of use thereof prior to the enactment date (July 12, 1960] with a view to prescribing a temporary tolerance or tolerances for such use or uses under paragraph (1)(C), the Secretary shall establish a temporary tolerance limitation at zero level for such use or uses until such time as he finds that it would not be inconsistent with the protection of the public health to increase or dispense with such temporary tolerance limitation. "SEC. 204. [EFFECT ON MEAT INSPECTION AND POULTRY PRODUCTS INSPECTION ACTS.] Nothing in this Act [amending this section and sections 321, 331, 333, 342, 343, 346, 351, 352, 361, 362, and 371 of this title and repealing sections 354 and 364 of this title] shall be construed to exempt any meat or meat food product, poultry or poultry product, or any person from any requirement imposed by or pursuant to the Meat Inspection Act of March 4, 1907, 34 Stat. 1260, as amended or extended (21 U.S.C. 71 and the following), or the Poultry Products Inspection Act (21 U.S.C. 451 and the following)." SHORT TITLE Section 1 of Pub. L. 86-618 provided that Pub. L. 86-618, which amended this section and sections 321, 331, 333, 342, 346, 351, 352, 361, 362, and 371 of this title, repealed section 354 and 364 of this title, and enacted notes set out under this section, may be cited as the "Color Additive Amendments of 1960." SUBCHAPTER VIII.-IMPORTS AND EXPORTS § 381. Imports and exports. The (a) Imports; list of registered foreign establishments; samples from unregistered foreign establishments; examination and refusal of admission. The Secretary of the Treasury shall deliver to the Secretary of Health, Education, and Welfare, upon his request, samples of food, drugs, devices, and cosmetics which are being imported or offered for import into the United States, giving notice thereof to the owner or consignee, who may appear before the Secretary of Health, Education, and Welfare and have the right to introduce testimony. Secretary of Health, Education, and Welfare shall furnish to the Secretary of the Treasury a list of establishments registered pursuant to section 360(i) of this title and shall request that if any drugs manufactured, prepared, propagated, compounded, or processed in an establishment not so registered are imported or offered for import into the United States, samples of such drugs be delivered to the Secretary of Health, Education, and Welfare, with notice of such delivery to the owner or consignee, who may appear before the Secretary of Health, Education, and Welfare and have the right to introduce testimony. If it appears from the examination of such samples or otherwise that (1) such article has been manufactured, processed, or packed under insanitary conditions, or (2) such article is forbidden or restricted in sale in the country in which it was produced or from which it was exported, or (3) such article is adulterated, misbranded, or in violation of section 355 of this title, then such article shall be refused admission, except as provided in subsection (b) of this section. The Secretary of the Treasury shall cause the destruction of any such article refused admission unless such article is exported, under regulations prescribed by the Secretary of the Treasury, within ninety days of the date of notice of such refusal or within such additional time as may be permitted pursuant to such regulations. This subsection shall not be construed to prohibit the admission of narcotic drugs the importation of which is permitted under section 173 of this title. (As amended Oct. 10, 1962, Pub. L. 87-781, title III, § 306, 76 Stat. 796.) REFERENCES IN TEXT "Section 173 of this title", as used at the end of subsection (a) of this section, originally read, "section 2 of the act of May 26, 1922, as amended (U.S.C., 1934 edition, Title 21, sec. 173)." The act of May 26, 1922, 42 Stat. 596, was an act to amend the act of February 9, 1909, as amended, 35 Stat. 614. Section 173 of this title is based upon section 2 of the act of February 9, 1909, as amended. Section 2 of the act of February 9, 1909, was amended by, and set out as amended in quotation marks in section 1 of the act of May 26, 1922. Section 2 of the act of May 26, 1922, amended sections 5 and 6 of the act of Februray 9, 1909, which are set out as sections 180 and 182 of this title. AMENDMENTS 1962 Subsec. (a). Pub. L. 87-781 inserted provisions requiring the Secretary of Health, Education, and Welfare to furnish the Secretary of the Treasury a list of establishments registered under section 360 (1) of this title, and to request that samples of any drugs from any establishments not so registered be delivered to the Secretary of Health, Education, and Welfare, with notice of delivery to the consignee who may appear before the Secretary to testify. SUBCHAPTER IX.-MISCELLANEOUS § 392. Exemption of meats and meat food products; laws unaffected. (a) Meats and meat food products shall be exempt from the provisions of this chapter to the extent of the application or the extension thereto of the Meat Inspection Act, approved March 4, 1907, as amended. (b) Nothing contained in this chapter shall be construed as in any way affecting, modifying, repealing, or superseding the provisions of the virus, serum, and toxin Act of July 1, 1902; the Filled Cheese Act of June 6, 1896, the Filled Milk Act of March 4, 1923; or the Import Milk Act of February 15, 1927. (June 25, 1938, ch. 675, § 902 (b), (c), 52 Stat. 1059.) REFERENCES IN TEXT The Meat Inspection Act, approved March 4, 1907, as amended, referred to in subsec. (a), is classified to sections 71-91 of this title. The virus, serum, and toxin act of July 1, 1902, referred to in subsec. (b), was formerly classified to sections 141148 of Title 42, The Public Health and Welfare, and was repealed by act July 1, 1944, ch. 373, title VIII, § 813, 58 Stat. 714. The Filled Cheese Act of June 6, 1896, referred to in subsec. (b), is now covered by section 4831 et seq. of Title 26, Internal Revenue Code of 1954. The Filled Milk Act of March 4, 1923, referred to in subsec. (b), is classified to chapter 3 of this title. The Import Milk Act of February 15, 1927, referred to in subsec. (b), is classified to sections 141-149 of this title. after the date of its enactment [June 25, 1938]. The Federal Food and Drugs Act of June 30, 1906, as amended (U.S.C., 1934 ed., title 21, secs. 1-15), shall remain in force until such effective date, and, except as otherwise provided in this subsection, is hereby repealed effective upon such date: Provided, That the provisions of section 701 [section 371 of this title] shall become effective on the enactment of this Act, and thereafter the Secretary is authorized hereby to (1) conduct hearings and to promulgate regulations which shall become effective on or after the effective date of this Act as the Secretary shall direct, and (2) designate prior to the effective date of this Act food having common or usual names and exempt such food from the requirements of clause (2) of section 403(1) [section 343(1) of this title] for a reasonable time to permit the formulation, promulgation, and effective application of definitions and standards of identity therefor as provided by section 401 [section 341 of this title]: Provided further, That sections 502(1), 505, and 601(a) [sections 352(j), 355, 361(a), respectively of this title], and all other provisions of this Act to the extent that they may relate to the enforcement of such sections, shall take effect on the date of the enactment of this Act, except that in the case of a cosmetic to which the proviso of section 601(a) [section 361(a) of this title], relates, such cosmetic shall not, prior to the ninetieth day after such date of enactment, be deemed adulterated by reason of the failure of its label to bear the legend prescribed in such proviso: Provided further, That the Act of March 4, 1923 (U.S.C., 1934 ed., title 21, sec. 6 [now section 321(a) of this title]; 42 Stat. 1500, ch. 268), defining butter and providing a standard therefor; the Act of July 24, 1919 (U.S.C., 1934 ed., title 21, sec. 10 [now section 321(b) of this title]; 41 Stat. 271, ch. 26), defining wrapped meats as in package form; and the amendment to the Food and Drugs Act, section 10A, approved August 27, 1935 (U.S.C. 1934 ed., Sup. III, title 21, sec. 14a [now section 372a of this title]), shall remain in force and effect and be applicable to the provisions of this Act." AVAILABILITY OF APPROPRIATIONS Section 902(d) of act June 25, 1938, provided that: "In order to carry out the provisions of this Act [affecting sections 1-15, 301 et seq. of this title] which take effect prior to the repeal of the Food and Drugs Act of June 30, 1906, as amended [sections 1-15 of this title], appropriations available for the enforcement of such Act of June 30, 1906, are also authorized to be made available to carry out such provisions." 508. (b) Procedure. Seizure of narcotic drugs, order forms, and tax stamps upon suspension or revocation of license. 509. Manufacturing quotas for basic classes of narcotic drugs. (a) Determination of quantity of drugs. (c) Application for quota; formula; minimum (d) Provisional quota for licensed manufacturers. (e) Application for quota by licensed manufacturer who has not manufactured basic class of drug, during one or more of three preceding years. (f) Increase of quota; matters considered. 510. Exception from applicability of license and quota provisions. 511. Records and reports by manufacturers of narcotic precursors; report to the Congress. Judicial review. 512. 513. 514. 515. 516. 517. Authorization by Secretary for importation of Enforcement and authority to delegate functions. Burden of proof of exemptions; presumptions. § 501. Congressional statement of purpose. The enactment of this chapter is necessary for the following reasons: (1) The Congress has long recognized that the manufacture, distribution, and use of narcotic drugs for nonmedical and nonscientific purposes endangers the health of the American people and threatens the general welfare. The Congress has enacted laws and the Senate has approved international conventions designed to establish effective control over domestic and international traffic in narcotic drugs. (2) Until recently, most narcotic drugs were made from natural raw materials such as the opium poppy and the coca leaf, produced in limited areas of the world. In practice, control over the production of narcotic drugs could therefore be achieved by national and international restrictions over the production and shipment of these raw materials and their use to manufacture narcotic drugs. (3) In recent years, however, technological advances have resulted in the development of new types of narcotic drugs, produced synthetically from a variety of generally available raw materials. As a result, controls over the production of narcotic drugs can no longer be maintained solely by controls relating to the opium poppy and the coca leaf. (4) The United States has joined with other nations in executing international conventions intended to establish suitable controls over production, ship These conven ment, and use of all narcotic drugs. tions are not self-executing, and the obligations of the United States thereunder must be performed pursuant to appropriate legislation. (5) In order (A) to discharge more effectively the international obligations of the United States, (B) to promote the public health, safety, and welfare, (C) to regulate interstate and foreign commerce in narcotic drugs, and (D) to safeguard the revenue derived from taxation of narcotic drugs, the Congress finds it necessary to enact a statute for the licensing and control of the manufacture of all narcotic drugs. (Pub. L. 86-429, § 2, Apr. 22, 1960, 74 Stat. 55.) REFERENCES IN TEXT This chapter, referred to in the text, was in the original "this Act", meaning Pub. L. 86-429, which added this chapter and amended section 182 of this title and sections 4702(a) and 4731 (a), (g) of Title 26, Internal Revenue Code of 1954. EFFECTIVE DATE Section 22 of Pub. L. 86-429 provided that: "With the exception of section 8(a) [section 506(a) of this title], this Act [adding this chapter, amending section 182 of this title and sections 4702(a), and 4731 (a), (g) of Title 26, and enacting notes set out under this section and section 4731 of Title 26] shall take effect on January 1 of the year following the date of its enactment [April 22, 1960]. Section 8(a) [section 506(a) of this title] shall take effect on the date of enactment of this Act [April 22, 1960]." SHORT TITLE Section 1 of Pub. L. 86-429 provided that Pub. L. 86429, which added this chapter, amended section 182 of this title and sections 4702(a) and 4731(a), (g) of Title 26, Internal Revenue Code of 1954, and enacted notes set out under this section and section 4731 of Title 26, may be cited as the "Narcotics Manufacturing Act of 1960." SEPARABILITY OF PROVISIONS Section 21 of Pub. L. 86-429 provided that: "If any provision of this Act [adding this chapter, amending section 182 of this title and sections 4702(a), and 4731 (a), (g) of Title 26, and enacting notes set out under this section and section 4731 of Title 26], or the application of such provision to any circumstances, shall be held invalid, the validity of the remainder of the Act and the applicability of such provision to other persons or circumstances shall not be affected thereby." § 502. Definitions. For the purposes of this chapter (a) The term "1931 convention" means the Convention for Limiting the Manufacture and Regulating the Distribution of Narcotic Drugs, concluded at Geneva, July 13, 1931, and entered into force with respect to the United States of America, July 9, 1933, as amended by the protocol signed at Lake Success on December 11, 1946. (b) The term "1948 protocol" means the protocol bringing under international control drugs outside the scope of the convention of July 13, 1931, for limiting the manufacture and regulating the distribution of narcotic drugs (as amended by the protocol signed at Lake Success on December 11, 1946), signed at Paris, November 19, 1948, and entered into force with respect to the United States of America, September 11, 1950. (c) The term "Secretary or his delegate" means the Secretary of the Treasury, or any officer, employee, or agency of the Treasury Department duly authorized by the Secretary (directly or indirectly by one or more redelegations of authority) to perform the function mentioned or described in the context. (d) The term "person" includes an individual, partnership, corporation, association, trust, or other institution or entity. (e) The term "narcotic drug" means narcotic drug as defined in section 4731(a) of Title 26, as amended by section 4 of this Act. (f) The term "manufacture" means the production of a narcotic drug, either directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis or by a combination of extraction and chemical synthesis. (g) The term "basic class of narcotic drug" means any one of the following classes of narcotic drugs and any additional class or classes of narcotic drugs (other than crude opium or coca leaves), by whatever trade name designated, as may be defined from time to time by the Secretary or his delegate in accordance with section 504 of this title: 1. Opium, powdered, granulated, or deodorized, or tinctures or extracts of opium. 2. Mixed alkaloids of opium and their salts. 10. Ethylmorphine and its salts. salts. (N-allylnormorphine) and its 13. Hydromorphone (dihydromorphinone) and its salts. 14. Metopon (methyldihydromorphinone) and its salts. 15. Dihydrocodeine and its salts. 16. Hydrocodone (dihydrocodeinone) and its salts. 17. Oxycodone (dihydrohydroxycodeinone) and its salts. 18. Cocaine and its salts. 19. Ecgonine and its salts. 20. Pethidine (meperidine, isonipecaine) (1methyl-4-phenylpiperidine-4-carboxylic acid ethyl ester) and its salts. 21. Alphaprodine (alpha-1, 3-dimethyl-4-phenyl4-propionoxypiperidine) and its salts. 22. Methadone (amidone) (6-dimethylamino-4, 4diphenyl-3-heptanone) and its salts. 23. Isomethadone (isoamidone) 6-dimethylamino5-methyl-4, 4-diphenyl-3-hexanone) and its salts. 24. Levorphan and racemorphan (3-hydroxy-Nmethylmorphinan) and their salts. 25. Levomethorphan and racemethorphan (3methoxy-N-methylmorphinan) and their salts. 26. Anileridine (Ethyl 1-[2-(p-amino phenyl)ethyl]-4-phenyl piperidine-4-carboxylate) and its |