MODERN Labeling Act of 2020
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Making Objective Drug Evidence Revisions for New Labeling Act of 2020 or the MODERN Labeling Act of 2020
This bill authorizes the Food and Drug Administration (FDA) to require updates to outdated labels for certain generic drugs if the updates will provide a public health benefit. Generally, the FDA may use this authority to update the label of a generic version of a brand-name drug that has been withdrawn from the market for reasons other than safety or effectiveness.
Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
- Engrossed in House Formatted Text PDF Formatted XML
- Introduced in House Formatted Text PDF Formatted XML
- Referred in Senate Formatted Text PDF Formatted XML
- Reported in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 5668: MODERN Labeling Act of 2020. 116th Congress. Open America. https://openamerica.io/bill/116-HR-5668/
"H.R. 5668: MODERN Labeling Act of 2020." 116th Congress, 2026, Open America, https://openamerica.io/bill/116-HR-5668/.
H.R. 5668, 116th Cong. (2026), https://openamerica.io/bill/116-HR-5668/.
[H.R. 5668: MODERN Labeling Act of 2020](https://openamerica.io/bill/116-HR-5668/)