[Congressional Bills 112th Congress]
[From the U.S. Government Publishing Office]
[S. 373 Introduced in Senate (IS)]

112th CONGRESS
  1st Session
                                 S. 373

   To amend the Federal Food, Drug, and Cosmetic Act to prohibit the 
                 marketing of authorized generic drugs.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                           February 16, 2011

Mr. Rockefeller (for himself, Mrs. Shaheen, Mr. Leahy, Mr. Inouye, Ms. 
  Stabenow, and Mr. Schumer) introduced the following bill; which was 
 read twice and referred to the Committee on Health, Education, Labor, 
                              and Pensions

_______________________________________________________________________

                                 A BILL


 
   To amend the Federal Food, Drug, and Cosmetic Act to prohibit the 
                 marketing of authorized generic drugs.

    Be it enacted by the Senate and House of Representatives of the 
United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

    This Act may be cited as the ``Fair Prescription Drug Competition 
Act''.

SEC. 2. PROHIBITION OF AUTHORIZED GENERICS.

    (a) In General.--Section 505 of the Federal Food, Drug, and 
Cosmetic Act (21 U.S.C. 355) is amended by adding at the end the 
following:
    ``(w) Prohibition of Authorized Generic Drugs.--
            ``(1) In general.--Notwithstanding any other provision of 
        this Act, no holder of a new drug application approved under 
        subsection (c) shall manufacture, market, sell, or distribute 
        an authorized generic drug, directly or indirectly, or 
        authorize any other person to manufacture, market, sell, or 
        distribute an authorized generic drug.
            ``(2) Authorized generic drug.--For purposes of this 
        subsection, the term `authorized generic drug'--
                    ``(A) means any version of a listed drug (as such 
                term is used in subsection (j)) that the holder of the 
                new drug application approved under subsection (c) for 
                that listed drug seeks to commence marketing, selling, 
                or distributing, directly or indirectly, after receipt 
                of a notice sent pursuant to subsection (j)(2)(B) with 
                respect to that listed drug; and
                    ``(B) does not include any drug to be marketed, 
                sold, or distributed--
                            ``(i) by an entity eligible for 180-day 
                        exclusivity with respect to such drug under 
                        subsection (j)(5)(B)(iv); or
                            ``(ii) after expiration or forfeiture of 
                        any 180-day exclusivity with respect to such 
                        drug under such subsection (j)(5)(B)(iv).''.
    (b) Conforming Amendment.--Section 505(t)(3) of the Federal Food, 
Drug, and Cosmetic Act (21 U.S.C. 355(t)(3)) is amended by striking 
``In this section'' and inserting ``In this subsection''.
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