Section 232 Tariffs Effective July 31 – Sept 29, 2026

Will Your Prescription
Cost More in 2026?

The US government is imposing up to a 100% tariff on brand-name drugs. Search your medication for instant tariff status.

Powered by OpenFDA + CMS NADAC government data · No account required

🏛FDA Drug Label API💊CMS NADAC Database📋White House Proclamation · Apr 2, 2026🔓No account required

Tariff Tiers

6 Rates. One Proclamation.

Full explainer →
100%

Default tariff

No deal, no exemption

20%

Onshoring plan

Committed to US production

15%

EU / Japan / Korea

Country-specific rate

10%

UK manufacturer

UK bilateral rate

0%

MFN deal (13 cos.)

Annex III company agreement

0%

Generic / exempt

Fully exempt — no tariff ever

100%

Default tariff

Brand-name patented drugs

13

MFN deal companies

Pay 0% under Annex III

0%

Tariff on generics

Fully exempt, always

FAQ

Common Questions

What Is the Section 232 Pharmaceutical Tariff?

On April 2, 2026, the Trump administration invoked Section 232 of the Trade Expansion Act of 1962 to impose tariffs on pharmaceutical imports. The default rate is 100% on all patented brand-name prescription drugs manufactured outside the United States without an approved exemption — the same authority previously used for steel and aluminum tariffs.

The tariff is structured into six tiers. Companies that signed MFN deals — including AbbVie, Eli Lilly, Merck, Novo Nordisk, Sanofi, and eight others — pay 0% with an earlier effective date of July 31, 2026.

Critically, generic drugs and biosimilars are entirely exempt. Since approximately 90% of all US prescriptions are filled with generics, the majority of patients are insulated from the tariff's direct effects. Use this tool to check your specific medication using real government data from OpenFDA and the CMS NADAC database.