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Authorized generics an interim report.

Washington, DC : Federal Trade Commission, 2009. 2009

Committee prints on administration legislative proposals on the Animal Drug User Fee Act Amendments

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2008. 2008

Expanding the use of generic drugs.

[Washington, D.C.] : Office of the Assistant Secretary for Planning and Evaluation, Office of Science and Data Policy, U.S. Department of Health and Human Services, 2010. 2010

H.R. 1706, the Protecting Consumer Access to Generic Drugs Act of 2009 hearing before the Subcommitt

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Commerce, Trade, and Consumer Protection.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2012. 2012

Making Objective Drug Evidence Revisions for New Labeling Act of 2020 : report (to accompany H.R. 56

United States. Congress. House. Committee on Energy and Commerce, author.
[Washington, D.C.] : [U.S. Government Publishing Office], [2020] 2020

Protecting Consumer Access to Generic Drugs Act of 2007 hearing before the Subcommittee on Commerce,

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Commerce, Trade, and Consumer Protection.
Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2007. 2007

Protecting Consumer Access to Generic Drugs Act of 2019 : report (to accompany H.R. 1499) (includin

United States. Congress. House. Committee on Energy and Commerce, author.
[Washington, D.C.] : [U.S. Government Publishing Office], [2019]- 2019