Data source

Data from U.S. Food & Drug Administration openFDA, delivered clean.

5 datasets pulled from U.S. Food & Drug Administration openFDA's releases, checked field by field and shipped the way you want them — daily, weekly, or hourly, your call.

  • 5 datasets
  • 1 industry
  • Real rows on request

What Datadory delivers from U.S. Food & Drug Administration openFDA

5
Pharmaceuticals United States regulatory scope · Adverse-event reports from Q3 2004 onward acc…

openFDA Drug APIs

Pharmaceuticals United States - concepts for products markete… · Release-stamped full-vocabulary snapshots

RxNorm / RxNav Browser and APIs

Pharmaceuticals International - the WHO global standard for d… · Annual editions

WHO ATC/DDD Index

Pharmaceuticals Global chemical literature and depositors · Continuously accumulating archive since its 2…

PubChem PUG REST API

Pharmaceuticals European Union and European Economic Area - m… · Current register snapshot per delivery

EMA Medicines Catalogue

Pick a catch, see the rows.

Name any U.S. Food & Drug Administration openFDA dataset and we send real rows from it — not a screenshot of rows. 1,744 datasets. Pick your catch.

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Straight answers about U.S. Food & Drug Administration openFDA data

How big is the FAERS adverse-event archive Datadory delivers?

20,692,690 reports in the slice counted at the 2026-08-17 export, accumulated quarterly since Q3 2004. Cases arrive as submitted reports - neither deduplicated nor clinically validated - so volume reads straight off the corpus while incidence math needs care.

How far down does the NDC Directory reach?

Package level. About 137,000 marketed products, each carrying labeler, brand and generic names, active ingredients with strengths, dosage form and route, plus child rows per package with their own codes and marketing start dates - one tube in one carton, literally.

Do the label documents include warning sections?

Yes - roughly 262,000 structured product labeling documents expose around ninety sections apiece, including indications and usage, boxed warning, drug interactions and dosage and administration, alongside the harmonized identifier block that ties each document to products and makers.

How far back do the approval histories run?

To 1939. Drugs@FDA contributes about 29,300 application records covering sponsors, submissions, marketing status and therapeutic-equivalence codes, with roughly 48,700 Orange Book approved-product entries sitting beside them for equivalence lookups.