About the bill
- Full Title
To permit manufacturers of generic drugs to provide additional warnings with respect to such drugs in the same manner that the Food and Drug Administration allows brand names to do so.
Legislative action may be ocurring on one of these bills in lieu of or in parallel to action on this bill.
Referred to Committee
Last Action: Apr 18, 2012
- What is a bill?
The “H.R.” in “H.R. 4384” means this is a House of Representatives bill in the United States Congress. A bill must be passed by both the House and Senate in identical form and then be signed by the President to become law.
The bill’s title was written by its sponsor.
- Committee Assignments
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There have been no votes related to this bill.
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Links & tools
Click a format for a citation suggestion:
Civic Impulse. (2015). H.R. 4384 — 112th Congress: Patient Safety and Drug Labeling Improvement Act. Retrieved from https://www.govtrack.us/congress/bills/112/hr4384
“H.R. 4384 — 112th Congress: Patient Safety and Drug Labeling Improvement Act.” www.GovTrack.us. 2012. May 23, 2015 <https://www.govtrack.us/congress/bills/112/hr4384>
|title=H.R. 4384 (112th)
|accessdate=May 23, 2015
|author=112th Congress (2012)
|date=April 18, 2012
|quote=Patient Safety and Drug Labeling Improvement Act