Every openFDA database, in one search.
30 datasets, 55,847,670 records: approvals, labels, NDCs, shortages, recalls, adverse event reports, device clearances and UDIs, substances, complete response letters and more. openFDA exported the newest on 2026-09-26.
Read today's FDA daily →State and federal rules by category →
Drugs
Approvals (Drugs@FDA) 29,350
Every FDA-approved drug and biologic application: sponsor, products, strengths and marketing status.
Searchable · updated 2026-09-26Orange Book 48,761
Approved drug products with therapeutic equivalence: reference listed drugs, reference standards and marketing status.
Searchable · updated 2026-09-26Drug labels 262,887
The full prescribing information and OTC labels (SPL): indications, dosing, warnings, boxed warnings and more.
Searchable · updated 2026-09-26NDC directory 138,259
Every drug listed with FDA by National Drug Code, including unfinished bulk ingredients, with packaging and labeler.
Searchable · updated 2026-09-26Drug shortages 1,601
FDA's drug shortage list: what is short, discontinued or resolved, by company and package, with the reason.
Searchable · updated 2026-09-26Drug recalls 17,975
Drug recall enforcement reports: the product, the firm, the reason and the recall class.
Searchable · updated 2026-09-25Drug adverse event reports (FAERS) 20,692,690
Reports of adverse events and medication errors sent to FDA for drugs and therapeutic biologics.
Searchable · updated 2026-09-23Devices
Device classification 7,093
Every device type FDA has classified: class, product code, regulation and whether it needs a 510(k) or PMA.
Searchable · updated 2026-09-23510(k) clearances 176,140
Premarket notifications FDA has decided: the device, the applicant, the decision and the product code.
Searchable · updated 2026-09-23PMA approvals 57,137
Premarket approvals for Class III devices and their supplements: trade name, applicant and decision.
Searchable · updated 2026-09-23Establishments and listings 335,617
Registered device establishments (makers, importers, repackagers) and the devices each one lists.
Searchable · updated 2026-09-23Device recalls 59,273
Device recalls with the root cause, the firm, the products and the recall status.
Searchable · updated 2026-09-25Device recall enforcement reports 39,969
The weekly enforcement reports for device recalls, with the recall class.
Searchable · updated 2026-09-25Unique 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 2026-09-23Device 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 2026-09-25COVID-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 2026-09-26Cosmetics
Food
Food recalls 29,415
Recall enforcement reports for foods and dietary supplements, with the recall class.
Searchable · updated 2026-09-25Food 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 2026-09-23Animal & veterinary
Tobacco
Tobacco product problem reports 1,383
Reports of health and product problems with tobacco products, including e-cigarettes.
Searchable · updated 2026-09-26Tobacco research: digital ads 12
Results from FDA's youth tobacco prevention digital ad research: views, attention and recognition per ad.
Browse · updated 2026-09-23Tobacco research: prevention ads 42
Perceived-effectiveness results for FDA tobacco prevention ads, by audience.
Browse · updated 2026-09-23Tobacco research: Smokefree.gov 22
Traffic and engagement measures for FDA's Smokefree.gov campaign pages.
Browse · updated 2026-09-23Substances & reference
Substances (GSRS) 167,385
FDA's Global Substance Registration System: every substance's names, identifiers, structure and relationships.
Searchable · updated 2026-09-23UNII codes 176,491
Unique Ingredient Identifiers: the code FDA assigns each ingredient, with its preferred name.
Searchable · updated 2026-09-26NDC SPL data elements 668,995
Every package NDC listed in drug labeling, with its marketing category, dates and application number.
Searchable · updated 2026-09-26Historical FDA documents 8,858
FDA press releases and papers from the agency's history, as full text.
Searchable · updated 2026-09-23Transparency
Research
Join free with your NPI to buy from vendors whose licenses MedGrid has reviewed, at wholesale pricing.
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.