H.R.749 - Lower Drug Costs through Competition Act115th Congress (2017-2018) |
|Sponsor:||Rep. Schrader, Kurt [D-OR-5] (Introduced 01/30/2017)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 02/03/2017 Referred to the Subcommittee on Health. (All Actions)|
This bill has the status Introduced
Here are the steps for Status of Legislation:
- Passed House
- Passed Senate
- To President
- Became Law
Summary: H.R.749 — 115th Congress (2017-2018)All Information (Except Text)
Introduced in House (01/30/2017)
Lower Drug Costs through Competition Act
This bill amends the Federal Food, Drug, and Cosmetic Act to revise provisions regarding review and approval of generic drug applications or supplements to generic drug applications for drugs: (1) for which there is a shortage, or (2) that have not been recently introduced to the market by more than one manufacturer and for which tentative approval has not been granted to more than two applications.
The Food and Drug Administration (FDA) must prioritize the review of such submissions and act on them within 180 days. The FDA may expedite the inspection of a facility proposed to manufacture such a drug.
Beginning FY2019, the FDA must award a transferrable generic drug priority review voucher to the sponsor of such an application once the drug has a sustained market presence. A voucher may be used to have the FDA review and take action upon a generic drug application within 180 days of submission. The FDA must establish an additional user fee for applications subject to a voucher. This voucher program is terminated at the start of FY2024.
The FDA must periodically report on generic drug applications filed before FY2018 that are still pending.
For a new drug application to be eligible for a priority review voucher as a tropical disease product application, the application must include new, essential clinical investigations.The Government Accountability Office must study the FDA's program for drug risk evaluation and mitigation strategies.