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Full Text of this Amendment

SA 1061. Mr. DORGAN (for himself and Ms. Snowe) submitted an amendment intended to be proposed by him to the bill S. 1082, to amend the Federal Food, Drug, and Cosmetic Act to reauthorize and amend the prescription drug user fee provisions, and for other purposes; which was ordered to lie on the table; as follows:
At the appropriate place in the amendment, insert the following:
SEC. __. COUNTRY OF ORIGIN LABELING ON PRESCRIPTION DRUGS.
(a) In General.--Not later than 90 days after the date of enactment of this Act, the Secretary of Health and Human Services shall issue regulations to require that the labeling, including retail packaging, of each prescription drug include the name of the country in which such prescription drug was manufactured.
(b) Definition.--In this section, the term ``labeling'' has the meaning given such term in section 201(m) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(m)).


(As printed in the Congressional Record for the Senate on May 8, 2007.)