US HB4384 | 2011-2012 | 112th Congress
Status
Spectrum: Partisan Bill (Democrat 2-0)
Status: Introduced on April 18 2012 - 25% progression, died in committee
Action: 2012-04-20 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on April 18 2012 - 25% progression, died in committee
Action: 2012-04-20 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Patient Safety and Drug Labeling Improvement Act - Amends the Federal Food, Drug, and Cosmetic Act to allow the holder of an approved abbreviated new drug application (generic drug approval) to change the labeling of a drug so approved in the same manner authorized by regulation for the holder of an approved new drug application. Allows conforming changes to be ordered to the labeling of the equivalent listed drug and each drug approved under the abbreviated new drug application process that corresponds to such listed drug.
Title
Patient Safety and Drug Labeling Improvement Act
Sponsors
Sen. Chris Van Hollen [D-MD] | Rep. Bruce Braley [D-IA] |
History
Date | Chamber | Action |
---|---|---|
2012-04-20 | House | Referred to the Subcommittee on Health. |
2012-04-18 | House | Referred to the House Committee on Energy and Commerce. |
Same As/Similar To
SB2295 (Related) 2012-04-18 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2498)
Subjects
Consumer affairs
Drug safety, medical device, and laboratory regulation
Health
Health information and medical records
Prescription drugs
Drug safety, medical device, and laboratory regulation
Health
Health information and medical records
Prescription drugs
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/112th-congress/house-bill/4384/all-info |
Text | https://www.congress.gov/112/bills/hr4384/BILLS-112hr4384ih.pdf |