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FDA NDC Directory Scraper - Drug Products

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Extract US drug products from the FDA National Drug Code directory: brand and generic name, labeler, dosage form, route, active ingredients with strength, marketing category, application number, package NDCs and DailyMed label link. Filter by ingredient, labeler, dosage form and route. No API key.

Pricing

from $1.00 / 1,000 result exporteds

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Ryan Zinburg

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3 days ago

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FDA NDC Directory Scraper - US Drug Product Database

Extract the National Drug Code directory, the FDA's list of every drug product marketed in the United States: brand and generic name, labeler, dosage form, route, active ingredients with strength, marketing dates and package codes.

Public openFDA source, no API key required, no proxy needed.

What you get per product

Field	Example
`productNdc`	0002-1433
`brandName`, `genericName`	Trulicity, dulaglutide
`labelerName`	Eli Lilly and Company
`productType`	HUMAN PRESCRIPTION DRUG, HUMAN OTC DRUG
`dosageForm`	INJECTION, SOLUTION
`routes`	["SUBCUTANEOUS"]
`activeIngredients`	["DULAGLUTIDE 1.5 mg/0.5mL"]
`ingredientNames`, `ingredientCount`	normalised ingredient list
`marketingCategory`	NDA, ANDA, OTC monograph
`applicationNumber`	NDA125469
`marketingStartDate`, `marketingEndDate`, `listingExpirationDate`	lifecycle dates
`packageNdcs`, `packageDescriptions`, `packageCount`	every package size
`pharmClasses`	established pharmacologic classes
`labelUrl`	link to the DailyMed label

brandName - e.g. Trulicity
genericName - e.g. dulaglutide
activeIngredient - ingredient name, e.g. metformin hydrochloride
labeler - manufacturer or labeler, e.g. Teva
dosageForm - e.g. TABLET, INJECTION, SOLUTION
route - e.g. ORAL, INTRAVENOUS
productType - prescription, OTC or other
marketingCategory - e.g. NDA, ANDA, OTC MONOGRAPH DRUG
productNdc - look up one specific product code
maxResults - up to 5000 products per run

Example input

{
  "genericName": "metformin hydrochloride",
  "productType": "HUMAN PRESCRIPTION DRUG",
  "maxResults": 500
}

Use cases

Pharmacy and formulary management - build a current product list per ingredient with all package codes
Generic competition analysis - see how many labelers market the same molecule and since when
Healthcare data integration - map NDC codes to names, strengths and dosage forms
Market entry research - check which dosage forms and routes already exist for an ingredient
Supply chain and procurement - resolve package NDCs to product details
Regulatory research - trace products back to their NDA or ANDA application number

Why the NDC directory

Listing a drug product with the FDA is mandatory before it can be marketed in the United States, so the NDC directory is the authoritative product master. openFDA republishes it with normalised fields and daily updates, free for any use.

Notes

The directory lists products, not packages. One product can carry several package NDCs, all included in packageNdcs.
marketingEndDate is only present for products that have been withdrawn or delisted.
openFDA refuses offsets beyond 25 000 records; narrow the filters to reach deeper.

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