US HB2562 | 2017-2018 | 115th Congress
Status
Spectrum: Partisan Bill (Republican 1-0)
Status: Introduced on May 19 2017 - 25% progression, died in committee
Action: 2017-05-26 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on May 19 2017 - 25% progression, died in committee
Action: 2017-05-26 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Making Pharmaceutical Markets More Competitive Act This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to prioritize the review of generic drug applications and supplements with respect to drugs that are in a shortage or for which there are not more than three approved drugs. The holder of an approved drug application must notify the FDA within 180 days of withdrawing or transferring the application or withdrawing the drug from sale. The FDA must maintain a list of generic drugs with three or fewer holders of approved applications.
Title
Making Pharmaceutical Markets More Competitive Act
Sponsors
Rep. Mike Kelly [R-PA] |
History
Date | Chamber | Action |
---|---|---|
2017-05-26 | House | Referred to the Subcommittee on Health. |
2017-05-19 | House | Referred to the House Committee on Energy and Commerce. |
2017-05-19 | House | Introduced in House |
Same As/Similar To
SB934 (Related) 2017-05-11 - Placed on Senate Legislative Calendar under General Orders. Calendar No. 76.
SB1115 (Same As) 2017-05-11 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
SB1115 (Same As) 2017-05-11 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Subjects
Administrative remedies
Congressional oversight
Department of Health and Human Services
Drug safety, medical device, and laboratory regulation
Government information and archives
Health
Prescription drugs
Congressional oversight
Department of Health and Human Services
Drug safety, medical device, and laboratory regulation
Government information and archives
Health
Prescription drugs
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/115th-congress/house-bill/2562/all-info |
Text | https://www.congress.gov/115/bills/hr2562/BILLS-115hr2562ih.pdf |