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Updated Drug Labeling for Patient Safety Act

USA117th CongressHR-9011| House 
| Updated: 9/29/2022
A. Donald McEachin

A. Donald McEachin

Democratic Representative

Virginia

Health Subcommittee, Energy and Commerce Committee

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Updated Drug Labeling for Patient Safety Act This bill allows generic drug manufacturers to revise labels with updated safety information that differs from the referenced brand-name drug.
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Timeline
Sep 28, 2022
Introduced in House
Sep 28, 2022
Referred to the House Committee on Energy and Commerce.
Sep 29, 2022
Referred to the Subcommittee on Health.
  • September 28, 2022
    Introduced in House


  • September 28, 2022
    Referred to the House Committee on Energy and Commerce.


  • September 29, 2022
    Referred to the Subcommittee on Health.

Health

Administrative law and regulatory proceduresDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationPrescription drugs

Updated Drug Labeling for Patient Safety Act

USA117th CongressHR-9011| House 
| Updated: 9/29/2022
Updated Drug Labeling for Patient Safety Act This bill allows generic drug manufacturers to revise labels with updated safety information that differs from the referenced brand-name drug.
View Full Text

Suggested Questions

Get AI-generated questions to help you understand this bill better

Timeline
Sep 28, 2022
Introduced in House
Sep 28, 2022
Referred to the House Committee on Energy and Commerce.
Sep 29, 2022
Referred to the Subcommittee on Health.
  • September 28, 2022
    Introduced in House


  • September 28, 2022
    Referred to the House Committee on Energy and Commerce.


  • September 29, 2022
    Referred to the Subcommittee on Health.
A. Donald McEachin

A. Donald McEachin

Democratic Representative

Virginia

Health Subcommittee, Energy and Commerce Committee

Health

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Administrative law and regulatory proceduresDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationPrescription drugs