H.R. 573 (111th): To amend the Federal Food, Drug, and Cosmetic Act to prohibit the marketing of authorized generic drugs.

Introduced:
Jan 15, 2009 (111th Congress, 2009–2010)
Sponsor:
Rep. Jo Ann Emerson [R-MO8]
Status:
Died (Referred to Committee)
See Instead:
This bill was re-introduced as H.R. 741 (112th) on Feb 16, 2011.

The bill’s title was written by the bill’s sponsor. H.R. stands for House of Representatives bill.

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Status

This bill was introduced on January 15, 2009, in a previous session of Congress, but was not enacted.

Progress
Introduced Jan 15, 2009
Cosponsors
3 cosponsors (2D, 1R) (show)
Committees

House Energy and Commerce

The committee chair determines whether a bill will move past the committee stage.

Summary

No summaries available.

Text

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Last updated Jan 15, 2009.
2 pages

Primary Source

View on THOMAS (The Library of Congress)

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GovTrack’s Bill Summary

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Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.

1/15/2009--Introduced.
Amends the Federal Food, Drug, and Cosmetic Act to prohibit a holder of a new, approved drug application from commencing to manufacture, market, sell, or distribute a generic version of such drug from the time of the receipt of notice from the generic manufacturer that an abbreviated new drug application has been submitted for approval until the expiration or forfeiture of the exclusivity period granted to the generic manufacturer.

House Republican Conference Summary

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No summary available.

House Democratic Caucus Summary

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The bill contains the following citations to other parts of U.S. law:

United States Code

The United States Code is the compilation of permanent laws enacted by Congress. Temporary and other non-permanent laws do not appear in the United States Code. (About half of the United States Code is the law itself, called positive law. The other half is merely a compilation of the laws but has no legal significance.)

  • Title 21: FOOD AND DRUGS
  • Chapter 9: FEDERAL FOOD, DRUG, AND COSMETIC ACT
  • Subchapter V: DRUGS AND DEVICES
  • Part A: Drugs and Devices
  • Section 355: New drugs