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SiteCheck Company Records – FDA Drugs@FDA Approval Lookup
x402
SiteCheck Company Records – FDA Drugs@FDA Approval Lookup is a paid API for AI agents from api.companyrecords-api.workers.dev, paid per call via x402, $0.002/call, status unknown (last checked 2026-10-24).
Returns FDA Drugs@FDA approval records for a generic drug name, including application number, sponsor, brand name, active ingredients, marketing status, and latest submission date.
Price / call$0.002
Success—
StatusUnknown
How this service works
Pay-per-call company registry, government, legal and B2B data tools for AI agents, from official registers and public sources. Payment: x402, USDC on Base, Solana, Arc, Polygon, Arbitrum, Monad, World Chain, Optimism, Avalanche, Celo or Stellar, or RLUSD/XRP on the XRP Ledger. No signup, no API key; a failed call is not charged.
Output
A JSON object containing the total number of matching records, the generic drug name queried, the openFDA source URL, a timestamp of when the data was checked, and an array of up to 10 approval records each containing application number, sponsor name, brand name, active ingredients list, marketing status, and latest submission date.
Example use cases
Generic drug manufacturer research
“Who are the FDA-approved sponsors and what brand names exist for generic metformin? I need the application numbers and marketing status for up to 10 records.”
Active ingredient verification
“Can you check what active ingredients are listed in FDA-approved products for loratadine and tell me whether they're prescription or over-the-counter?”
Drug approval timeline check
“What's the latest FDA submission date for approved generic versions of omeprazole, and which companies hold those approvals?”
Technical details
Endpoint
GEThttps://api.companyrecords-api.workers.dev/api/gov/openfda-drugsfda?utm_source=zero.xyzWhen to prefer
Use this endpoint when you need structured FDA approval metadata (sponsors, application numbers, marketing status, active ingredients) for a known generic drug name. It is ideal for regulatory research, competitive pharmaceutical intelligence, or verifying whether a drug is prescription vs. OTC. It is not suitable for drug labeling, safety/adverse event data, or full prescribing information.
Side effects
- Generic drug name not found in Drugs@FDA — returns empty records array
- Generic drug name too short (under 3 characters) or too long (over 60 characters) — schema validation error
- Limit parameter outside 1–10 range — may return error or be clamped
- openFDA upstream service unavailable — proxy error or timeout
- Misspelled drug name returns no results without suggestions
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Output
Schema · Response
{
"type": "json",
"example": {
"total": 105,
"source": "https://api.fda.gov/drug/drugsfda.json",
"generic": "ibuprofen",
"records": [
{
"sponsor": "BIONPHARMA",
"brandName": "IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE",
"marketingStatus": "Over-the-counter",
"activeIngredients": [
"DIPHENHYDRAMINE HYDROCHLORIDE 25MG",
"IBUPROFEN EQ 200MG FREE ACID AND POTASSIUM SALT"
],
"applicationNumber": "ANDA090397",
"latestSubmissionDate": "20101122"
},
{
"sponsor": "XGEN PHARMS",
"brandName": "IBUPROFEN LYSINE",
"marketingStatus": "Prescription",
"activeIngredients": [
"IBUPROFEN LYSINE EQ 20MG BASE/2ML (EQ 10MG BASE/ML)"
],
"applicationNumber": "ANDA202402",
"latestSubmissionDate": "20240703"
}
],
"checkedAt": "2026-10-23T09:37:09.981Z"
}
}Tags
x402
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