ABC Safe Drug Act
ABC Safe Drug Act
Plain Language Summary
# ABC Safe Drug Act Summary **What the Bill Would Do** The ABC Safe Drug Act would gradually reduce the federal government's purchases of medications containing active ingredients manufactured in China. Starting immediately, the bill phases in restrictions, with a complete ban taking effect by January 1, 2030, on any drugs with Chinese-sourced active ingredients unless they meet FDA safety standards. The bill also includes tax incentives to encourage pharmaceutical and medical device manufacturing in the United States, and requires all drugs to clearly label which country produced each active ingredient. **Who It Affects and Key Provisions** This bill primarily affects federal health care programs (like Medicare and Medicaid), pharmaceutical manufacturers, and potentially patients who take medications with Chinese-sourced ingredients. The Department of Health and Human Services can issue temporary waivers for programs that cannot meet the requirement, though this waiver authority expires in 2031.
Drugs without country-of-origin labeling would be considered misbranded and potentially removed from the market. The bill aims to address supply chain concerns by incentivizing domestic pharmaceutical production through tax benefits. **Current Status** As of now, the bill (S 1407) is in committee and has not yet been voted on by the full Senate. It was introduced in the 119th Congress by Senator Tom Cotton (R-AR).
CRS Official Summary
Anyone But China Safe Drug Act or the ABC Safe Drug ActThis bill restricts federal health care programs from purchasing drugs with active ingredients manufactured in China and provides tax incentives for the purchase of certain pharmaceutical and device manufacturing property for use in the United States.The bill phases in restrictions on federal health care programs’ purchase of drugs. By January 1, 2030, federal health care programs may not purchase any drug that contains active ingredients from China or countries that do not meet the health and safety standards of the Food and Drug Administration. The Department of Health and Human Services may issue a waiver for an agency or program that is unable to meet this requirement; this waiver authority expires in 2031. The bill also requires all drugs to be labeled with the country of origin of each active ingredient in the drug. Drugs that are not labeled with this information are deemed misbranded.Finally, the bill allows 100% tax expensing for qualified pharmaceutical and medical device manufacturing property placed in service between 2025 and 2030. Qualified pharmaceutical and medical device manufacturing property is any tangible property placed in service in the United States as part of the construction or expansion of property for the manufacture of drugs or devices.
Latest Action
Read twice and referred to the Committee on Finance.