United States· US:13267-345_5494a263-4c20-4f8d-9ce1-21705c4a8534
Fluorodopa
A medicinal product containing fluorodopa f-18, registered in United States by THE FEINSTEIN INSTITUTES FOR MEDICAL RESEARCH.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- FLUORODOPA F-18
- Manufacturer
- THE FEINSTEIN INSTITUTES FOR MEDICAL RESEARCH
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc11132673455625 mL in 1 VIAL, GLASS (13267-345-56)
- ndc1113267-345-56
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fluorodopa f-18 in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaFLUORODOPA (18F) BIONTBIONT a.s., Bratislava
- GermanyDoparosHelmholtz-Zentrum Dresden-Rossendorf Fwp
- SpainDOPACIS 90 MBq/ml SOLUCION INYECTABLECis Bio International
- FranceDOPACIS 90 MBq/mL, solution injectableCIS BIO INTERNATIONAL
- NetherlandsDopacis 90 MBq/ml, oplossing voor injectieCis Bio International
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Iasodopa
- Belgium · Fluorodopa (18f) Cis Bio International
- Czechia · Fluorodopa (18f) Ujv
- Germany · Doparos, Dopaview
- Spain · Dopacis, Dopaview
- France · Dopacis, Dopaview
- Hungary · Fdopa Kedoi
- Italy · Fluorodopa (18f) Curium Italy, Fluorodopa Iason
- Luxembourg · Dopacis
- Malta · Dopacis
- Netherlands · Dopacis
- Portugal · Dopacis, Dopaview
- Slovenia · Dopacis
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/d8e8c647-349b-4734-bd1d-c884bc82877e GET /v1/drugs/d8e8c647-349b-4734-bd1d-c884bc82877e?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "INTRAVENOUS",
"source": "ndc",
"strength": "8.33",
"substance": "FLUORODOPA F-18",
"productndc": "13267-345",
"dosage_form": "INJECTION",
"dea_schedule": null,
"strength_unit": "mCi/mL",
"application_number": "NDA200655",
"marketing_category": "NDA"
}See everything about fluorodopa f-18.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.