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Easier Approval for Generic Animal Drugs

New rules aim to simplify the market entry of generic animal drugs, potentially lowering prices and increasing availability. The changes focus on how these drugs are approved, especially regarding bioequivalence studies.
Key points
Streamlining the approval process for generic animal drugs, which could lead to more competition and lower costs.
Requiring proof of bioequivalence for generic drugs in at least one major animal species for which the original drug is approved.
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Expired
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Additional Information
Print number: 118_HR_1683
Sponsor: Rep. Mace, Nancy [R-SC-1]
Process start date: 2023-03-21
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Summarized by: gemini-2.5-flash-preview-05-20
Source data: api.congress.gov
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OFFICIAL LEGAL TITLE

Generic Animal Drug Advancement Act

FREQUENTLY ASKED QUESTIONS

What is the official ID of this bill?

The official print number for this legislation is 118_HR_1683.

Which chamber initiated this legislation?

This legislation was initiated in the House of Representatives.

When did the legislative process begin?

The process officially started on 2023-03-21.

What are the main provisions?

Key points include:

  • Streamlining the approval process for generic animal drugs, which could lead to more competition and lower costs.
  • Requiring proof of bioequivalence for generic drugs in at least one major animal species for which the original drug is approved.
What is the specific legal status?

The current status is Expired.

Where can I read the full text of this legislation?

The full official text is available at: View full text

Who is the primary sponsor?

The primary sponsor is Rep. Mace, Nancy [R-SC-1].

What is the latest detailed status?

The latest detailed status is: Referred to the Subcommittee on Health.

Is this summary verified?

Yes. This content was analyzed by AI and verified by the Lustra Judge System on 2025-12-24.

CATEGORIES

Health Agriculture