Preserving Access to Orphan Drugs Act of 2013
Official title: To clarify the orphan drug exception to the annual fee on branded prescription pharmaceutical manufacturers and importers.
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Rereferred to the Committee on Ways and Means, and in addition to the Committee on Energy and Commerce, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Preserving Access to Orphan Drugs Act of 2013 - Amends the Patient Protection and Affordable Care Act (PPACA) to exclude any drug or biological product which is approved or licensed by the Food and Drug Administration (FDA) for marketing solely for one or more rare diseases or conditions (orphan drug) from the annual fee on manufacturers or importers with branded prescription drug sales exceeding $5 million.
Makes this Act effective as if included in PPACA.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 2315: Preserving Access to Orphan Drugs Act of 2013. 113th Congress. Open America. https://openamerica.io/bill/113-HR-2315/
"H.R. 2315: Preserving Access to Orphan Drugs Act of 2013." 113th Congress, 2026, Open America, https://openamerica.io/bill/113-HR-2315/.
H.R. 2315, 113th Cong. (2026), https://openamerica.io/bill/113-HR-2315/.
[H.R. 2315: Preserving Access to Orphan Drugs Act of 2013](https://openamerica.io/bill/113-HR-2315/)