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Tariff Exclusions & Exemptions

Exclusions and exemptions under each measure: request windows, grants and denials, extensions and expiry, retroactive periods, and the Chapter 99 codes that claim an exclusion.

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Sep 22Tue
  1. Federal Register · BIS (EAR / Entity List)74

    BIS defines zero-tariff specialty pharmaceuticals and eligible jurisdictions under Proclamation 11020

    BIS issued a notice defining the pharmaceutical products and listing the jurisdictions eligible for a zero ad valorem Section 232 tariff rate under Proclamation 11020 of April 2, 2026, covering orphan-indication drugs and associated ingredients, nuclear medicines, plasma derived therapies, fertility drugs, cell therapy products, gene therapy products, antibody drug conjugates, chemical, biological, radiological and nuclear medical countermeasures, and animal health. Products and associated ingredients receive the zero rate if they are of a jurisdiction with a current or forthcoming trade and security framework agreement or meet an urgent U.S. health need.

    Why it matters: Importers of the listed pharmaceutical products and ingredients can seek the zero Section 232 rate by submitting urgent-health-need information to pharma232@bis.doc.gov on an ongoing basis from September 23, 2026.

Sep 1Tue
  1. Federal Register · USTR62

    USTR amends four Section 301 China product exclusions to conform to USITC HTSUS changes

    USTR is making conforming amendments to four product exclusions associated with the Section 301 investigation of China's acts, policies and practices related to technology transfer, intellectual property and innovation, after the USITC implemented changes to HTSUS statistical reporting categories effective July 1, 2026. The conforming amendments in the Annex to the notice are effective as of July 1, 2026. CBP will issue instructions on entry guidance and implementation.