Every openFDA database, in one search.
30 datasets, 55,850,846 records: approvals, labels, NDCs, shortages, recalls, adverse event reports, device clearances and UDIs, substances, complete response letters and more. openFDA exported the newest on 2026-10-05.
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Drugs
Approvals (Drugs@FDA) 29,379
Every FDA-approved drug and biologic application: sponsor, products, strengths and marketing status.
Searchable · updated 2026-10-05Orange Book 48,761
Approved drug products with therapeutic equivalence: reference listed drugs, reference standards and marketing status.
Searchable · updated 2026-10-05Drug labels 262,890
The full prescribing information and OTC labels (SPL): indications, dosing, warnings, boxed warnings and more.
Searchable · updated 2026-10-05NDC directory 138,239
Every drug listed with FDA by National Drug Code, including unfinished bulk ingredients, with packaging and labeler.
Searchable · updated 2026-10-05Drug shortages 1,590
FDA's drug shortage list: what is short, discontinued or resolved, by company and package, with the reason.
Searchable · updated 2026-10-05Drug recalls 18,002
Drug recall enforcement reports: the product, the firm, the reason and the recall class.
Searchable · updated 2026-10-05Drug adverse event reports (FAERS) 20,692,690
Reports of adverse events and medication errors sent to FDA for drugs and therapeutic biologics.
Searchable · updated 2026-10-05Devices
Device classification 7,094
Every device type FDA has classified: class, product code, regulation and whether it needs a 510(k) or PMA.
Searchable · updated 2026-10-05510(k) clearances 176,299
Premarket notifications FDA has decided: the device, the applicant, the decision and the product code.
Searchable · updated 2026-10-05PMA approvals 57,238
Premarket approvals for Class III devices and their supplements: trade name, applicant and decision.
Searchable · updated 2026-10-05Establishments and listings 336,250
Registered device establishments (makers, importers, repackagers) and the devices each one lists.
Searchable · updated 2026-10-05Device recalls 59,344
Device recalls with the root cause, the firm, the products and the recall status.
Searchable · updated 2026-10-05Device recall enforcement reports 40,113
The weekly enforcement reports for device recalls, with the recall class.
Searchable · updated 2026-10-05Unique device identifiers (GUDID) 5,182,695
The Global UDI Database: each device version's identifier, model, maker, sterility, MRI safety and latex labeling.
Searchable · updated 2026-10-05Device adverse event reports (MAUDE) 26,136,889
Medical device reports of deaths, injuries and malfunctions sent to FDA by makers, facilities and the public.
Searchable · updated 2026-10-05COVID-19 serology test evaluations 13,420
Independent evaluations of COVID-19 antibody tests: each sample's known result against the test's result.
Searchable · updated 2026-10-05Cosmetics
Food
Food recalls 29,471
Recall enforcement reports for foods and dietary supplements, with the recall class.
Searchable · updated 2026-10-05Food and supplement adverse event reports (CAERS) 151,589
Reports of adverse events and complaints for foods, dietary supplements and cosmetics sent to CFSAN.
Searchable · updated 2026-10-05Animal & veterinary
Tobacco
Tobacco product problem reports 1,383
Reports of health and product problems with tobacco products, including e-cigarettes.
Searchable · updated 2026-10-05Tobacco research: digital ads
Results from FDA's youth tobacco prevention digital ad research: views, attention and recognition per ad.
BrowseTobacco research: prevention ads
Perceived-effectiveness results for FDA tobacco prevention ads, by audience.
BrowseTobacco research: Smokefree.gov
Traffic and engagement measures for FDA's Smokefree.gov campaign pages.
BrowseSubstances & reference
Substances (GSRS) 167,385
FDA's Global Substance Registration System: every substance's names, identifiers, structure and relationships.
Searchable · updated 2026-10-05UNII codes 176,590
Unique Ingredient Identifiers: the code FDA assigns each ingredient, with its preferred name.
Searchable · updated 2026-10-05NDC SPL data elements 669,875
Every package NDC listed in drug labeling, with its marketing category, dates and application number.
Searchable · updated 2026-10-05Historical FDA documents 8,858
FDA press releases and papers from the agency's history, as full text.
Searchable · updated 2026-10-02Transparency
Research
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.