To amend the Federal Food, Drug, and Cosmetic Act to prohibit the marketing of authorized generic drugs.
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HR 573 — To amend the Federal Food, Drug, and Cosmetic Act to prohibit the marketing of authorized generic drugs.
Last action — Referred to the Subcommittee on Health.
No card. One bill, free forever — alerts when it moves.
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✓Introduced
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2In Committee
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3Passed House
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4Passed Senate
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5To Executive
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6Enacted
This bill died with 111th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
This bill is no longer active — its legislative session has ended, so there is no live prognosis. It would have to be reintroduced in the current session to move again.
Summary
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.
Bill Text
- Introduced Introduced in House Current html January 15, 2009
Action History
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Referred to the Subcommittee on Health.
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Referred to the House Committee on Energy and Commerce.
Sponsorship breakdown
Export CSV (upgrade) →0 sponsors · 0 co-sponsors · 547 not signed on
Sponsors (0)
None.
Co-sponsors (0)
None.
Not signed on (547)
547 members have not signed on to this bill.
Show all 547 →"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.
Subjects
Frequently asked questions
- What does HR 573 do?
- 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.
- What is the current status of HR 573?
- This bill died with 111th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
- Where can I track HR 573?
- Track HR 573 free on One Click Politics — get push/email alerts when it moves.
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Last checked for changes 13 days ago · updated continuously
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