Modern Authentication of Pharmaceuticals Act of 2025
Official title: To amend the Federal Food, Drug, and Cosmetic Act to modernize the methods of authenticating controlled substances in the pharmaceutical distribution supply chain, and for other purposes.
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Referred to the House Committee on Energy and Commerce.
Modern Authentication of Pharmaceuticals Act of 2025
This bill requires each dose of a pharmaceutical product that is a controlled substance and that is taken orally in solid form (i.e., pills) to include a physical chemical identifier. (Physical chemical identifiers are substances that possess a unique physical or chemical property, such as inks, pigments, flavors, and molecular taggants, that unequivocally identify and authenticate a drug or dosage.) Under the bill, physical chemical identifiers must be included in or on the product and must be machine readable.
The bill applies to products manufactured beginning five years after the bill's enactment.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 1060: Modern Authentication of Pharmaceuticals Act of 2025. 119th Congress. Open America. https://openamerica.io/bill/119-HR-1060/
"H.R. 1060: Modern Authentication of Pharmaceuticals Act of 2025." 119th Congress, 2026, Open America, https://openamerica.io/bill/119-HR-1060/.
H.R. 1060, 119th Cong. (2026), https://openamerica.io/bill/119-HR-1060/.
[H.R. 1060: Modern Authentication of Pharmaceuticals Act of 2025](https://openamerica.io/bill/119-HR-1060/)