Sec. 2. SCHEDULING OF SUBSTANCES INCLUDED IN NEW FDA-APPROVED DRUGS

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## SEC. 2 SCHEDULING OF SUBSTANCES INCLUDED IN NEW FDA-APPROVED DRUGS ###

(a)Effective Date of Approval ####

(1)Effective date of drug approval Section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355) is amended by adding at the end the following: > > ### “(x) Date of Approval in the Case of Recommended Controls Under the CSA > > > #### “(1) In general > > In the case of an application under subsection

(b)with respect to a drug for which the Secretary provides notice to the sponsor that the Secretary intends to issue a scientific and medical evaluation and recommend controls under the Controlled Substances Act, approval of such application shall not take effect until the interim final rule controlling the drug is issued in accordance with section 201(j) of the Controlled Substances Act. > > > #### “(2) Date of approval > > For purposes of this section, with respect to an application described in paragraph (1), the term ‘date of approval’ shall mean the later of— > > > ##### “(A) > > the date an application under subsection

(b)is approved under subsection (c); or > > > ##### “(B) > > the date of issuance of the interim final rule controlling the drug.” > . ####

(2)Effective date of approval of biological products Section 351 of the Public Health Service Act (42 U.S.C. 262) is amended by adding at the end the following: > > ### “(n) Date of Approval in the Case of Recommended Controls Under the CSA > > > #### “(1) In general > > In the case of an application under subsection

(a)with respect to a biological product for which the Secretary provides notice to the sponsor that the Secretary intends to issue a scientific and medical evaluation and recommend controls under the Controlled Substances Act, approval of such application shall not take effect until the interim final rule controlling the biological product is issued in accordance with section 201(j) of the Controlled Substances Act. > > > #### “(2) Date of approval > > For purposes of this section, with respect to an application described in paragraph (1), references to the date of approval of such application, or licensure of the product subject to such application, shall mean the later of— > > > ##### “(A) > > the date an application is approved under subsection (a); or > > > ##### “(B) > > the date of issuance of the interim final rule controlling the biological product.” > . ####

(3)Effective date of approval of animal drugs #####

(A)In general Section 512 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360b) is amended by adding at the end the following: > > ### “(q) Date of Approval in the Case of Recommended Controls Under the CSA > > > #### “(1) In general > > In the case of an application under subsection

(b)is approved under subsection (c); or > > > ##### “(B) > > the date of issuance of the interim final rule controlling the drug.” > . #####

(B)Conditional approval Section 571(d) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360ccc(d)) is amended by adding at the end the following: > > #### “(4) > > > #####

(A)> > In the case of an application under subsection

(a)with respect to a drug for which the Secretary provides notice to the sponsor that the Secretary intends to issue a scientific and medical evaluation and recommend controls under the Controlled Substances Act, conditional approval of such application shall not take effect until the interim final rule controlling the drug is issued in accordance with section 201(j) of the Controlled Substances Act. > > > ##### “(B) > > For purposes of this section, with respect to an application described in subparagraph (A), the term ‘date of approval’ shall mean the later of— > > > ###### “(i) > > the date an application under subsection

(a)is conditionally approved under subsection (b); or > > > ###### “(ii) > > the date of issuance of the interim final rule controlling the drug.” > . #####

(C)Indexing of legally marketed unapproved new animal drugs Section 572 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360ccc-1) is amended by adding at the end the following: > > ### “(k) > > In the case of a request under subsection

(d)to add a drug to the index under subsection

(a)with respect to a drug for which the Secretary provides notice to the person filing the request that the Secretary intends to issue a scientific and medical evaluation and recommend controls under the Controlled Substances Act, a determination to grant the request to add such drug to the index shall not take effect until the interim final rule controlling the drug is issued in accordance with section 201(j) of the Controlled Substances Act.” > . ####

(4)Date of approval for designated new animal drugs Section 573(c) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360ccc-2(c)) is amended by adding at the end the following: > > #### “(3) > > For purposes of determining the 7-year period of exclusivity under paragraph

(1)for a drug for which the Secretary intends to issue a scientific and medical evaluation and recommend controls under the Controlled Substances Act, the drug shall not be considered approved or conditionally approved until the date that the interim final rule controlling the drug is issued in accordance with section 201(j) of the Controlled Substances Act.” > . ###

(b)Scheduling of Newly Approved Drugs Section 201 of the Controlled Substances Act (21 U.S.C. 811) is amended by inserting after subsection

(i)the following: > > ### “(j) > > > ####

(1)> > With respect to a drug referred to in subsection (f), if the Secretary of Health and Human Services recommends that the Attorney General control the drug in schedule II, III, IV, or V pursuant to subsections

(a)and (b), the Attorney General shall, not later than 90 days after the date described in paragraph (2), issue an interim final rule controlling the drug in accordance with such subsections and section 202(b) using the procedures described in paragraph (3). > > > #### “(2) > > The date described in this paragraph shall be the later of— > > > ##### “(A) > > the date on which the Attorney General receives the scientific and medical evaluation and the scheduling recommendation from the Secretary of Health and Human Services in accordance with subsection (b); or > > > ##### “(B) > > the date on which the Attorney General receives notification from the Secretary of Health and Human Services that the Secretary has approved an application under section 505(c), 512, or 571 of the Federal Food, Drug, and Cosmetic Act or section 351(a) of the Public Health Service Act, or indexed a drug under section 572 of the Federal Food, Drug, and Cosmetic Act, with respect to the drug described in paragraph (1). > > > #### “(3) > > A rule issued by the Attorney General under paragraph

(1)shall become immediately effective as an interim final rule without requiring the Attorney General to demonstrate good cause therefor. The interim final rule shall give interested persons the opportunity to comment and to request a hearing. After the conclusion of such proceedings, the Attorney General shall issue a final rule in accordance with the scheduling criteria of subsections (b), (c), and

(d)of this section and section 202(b).” > . ###

(c)Extension of Patent Term Section 156 of title 35, United States Code, is amended— ####

(1)in subsection (d)(1), in the matter preceding subparagraph (A), by inserting “, or in the case of a drug product described in subsection (i), within the sixty-day period beginning on the covered date (as defined in subsection (i))” after “marketing or use”; and ####

(2)by adding at the end the following: > > ### “(i) > > > ####

(1)> > For purposes of this section, if the Secretary of Health and Human Services provides notice to the sponsor of an application or request for approval, conditional approval, or indexing of a drug product for which the Secretary intends to recommend controls under the Controlled Substances Act, beginning on the covered date, the drug product shall be considered to— > > > ##### “(A) > > have been approved or indexed under the relevant provision of the Public Health Service Act or Federal Food, Drug, and Cosmetic Act; and > > > ##### “(B) > > have permission for commercial marketing or use. > > > #### “(2) > > In this subsection, the term ‘covered date’ means the later of— > > > ##### “(A) > > the date an application is approved— > > > ###### “(i) > > under section 351(a)(2)(C) of the Public Health Service Act; or > > > ###### “(ii) > > under section 505(b) or 512(c) of the Federal Food, Drug, and Cosmetic Act; > > > ##### “(B) > > the date an application is conditionally approved under section 571(b) of the Federal Food, Drug, and Cosmetic Act; > > > ##### “(C) > > the date a request for indexing is granted under section 572(d) of the Federal Food, Drug, and Cosmetic Act; or > > > ##### “(D) > > the date of issuance of the interim final rule controlling the drug under section 201(j) of the Controlled Substances Act.” > .

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Sec. 2

SCHEDULING OF SUBSTANCES INCLUDED IN NEW FDA-APPROVED DRUGS

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