S. 2295 (112th): Patient Safety and Generic Labeling Improvement Act

112th Congress, 2011–2013. Text as of Apr 18, 2012 (Introduced).

Status & Summary | PDF | Source: GPO

II

112th CONGRESS

2d Session

S. 2295

IN THE SENATE OF THE UNITED STATES

April 18, 2012

(for himself, Mr. Franken, Mr. Coons, Mr. Whitehouse, Mr. Bingaman, Mr. Brown of Ohio, and Mr. Blumenthal) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions

A BILL

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.

1.

Short title

This Act may be cited as the Patient Safety and Generic Labeling Improvement Act.

2.

Warning labeling with respect to generic drugs

Section 505(j) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)) is amended by adding at the end the following:

(11)
(A)

Notwithstanding any other provision of this Act, the holder of an approved application under this subsection may change the labeling of a drug so approved in the same manner authorized by regulation for the holder of an approved new drug application under subsection (b).

(B)

In the event of a labeling change made under subparagraph (A), the Secretary may order conforming changes to the labeling of the equivalent listed drug and each drug approved under this subsection that corresponds to such listed drug.

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