H.R. 5853 (112th): Gray Market Drug Reform and Transparency Act of 2012

Introduced:
May 22, 2012 (112th Congress, 2011–2013)
Sponsor:
Rep. Elijah Cummings [D-MD7]
Status:
Died (Referred to Committee)
See Instead:
This bill was re-introduced as H.R. 1958 on May 14, 2013. See H.R. 1958 for current action on this subject.

The bill’s title was written by the bill’s sponsor. H.R. stands for House of Representatives bill.

GovTrack’s Bill Summary

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Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


5/22/2012--Introduced.
Gray Market Drug Reform and Transparency Act of 2012 - Amends the Federal Food, Drug, and Cosmetic Act to:
(1) make it a prohibited act and a misbranding for a wholesale distributor of prescription drugs to purchase or receive a prescription drug from a pharmacy or a pharmacist,
(2) require annual reporting by wholesale distributors of prescription drugs,
(3) require the Secretary of Health and Human Services (HHS) to establish and maintain a national database of information reported by wholesale distributors of prescription drugs and to require such database to include information on actions taken by states against wholesale distributors (e.g., disciplinary actions and license revocations),
(4) require the Secretary to assess and collect fees from wholesale distributors of prescription drugs, and
(5) require wholesale distributors of prescription drugs to provide to recipients of a prescription drug in shortage the sales price for such drug at the time of its sale and at the time of any prior sale of such drug when it was in shortage.

House Republican Conference Summary

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No summary available.

House Democratic Caucus Summary

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The bill contains the following citations to other parts of U.S. law:

United States Code

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