List United States Drug Product Directory records
List United States Drug Product Directory records with optional filters and pagination.
Source: Source: openFDA, U.S. Food and Drug Administration. Not for clinical use. (Public domain (CC0, US Government work)).
Fields returned:
- product_ndc (str) — National drug code identifying the labeller and product
- brand_name (str) — Marketed brand or proprietary name
- generic_name (str) — Generic or non-proprietary name of the active ingredients
- labeler_name (str) — Company that labels and markets the product
- dosage_form (str) — Physical form, for example tablet, injection or cream
- product_type (str) — Whether the product is prescription, over-the-counter or another category
- marketing_category (str) — Regulatory pathway under which the product is marketed
- dea_schedule (str) — Controlled substance schedule where one applies
- marketing_start_date (str) — Date marketing began, formatted as YYYYMMDD
- finished (bool) — True for finished dosage products, false for bulk ingredients
Example: GET /v1/data/united-states-drug-product-directory?limit=10&labeler_name=example
Request
- Base URL: https://api.aristocles.com.au (the document declares no server; this is the origin it was published from)
- URL: https://api.aristocles.com.au/v1/data/united-states-drug-product-directory
- Auth: none declared. Required headers: X-API-Key
Query parameters
Max records to return (1-100).
Records to skip, for pagination.
Company that labels and markets the product
Physical form, for example tablet, injection or cream
Whether the product is prescription, over-the-counter or another category
Regulatory pathway under which the product is marketed
Controlled substance schedule where one applies
Headers
Response
A page of United States Drug Product Directory records with pagination metadata.
Changes
No recorded changes to this operation across all 2 revisions of this API.