United States· US:51759-202_4e729b85-d3b0-445d-9cba-9326b4e2291f
AJOVY
A fremanezumab product containing fremanezumab, registered in United States by Teva Pharmaceuticals USA, Inc.. The same ATC class is registered in 15 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Fremanezumab is registered in 15 of 19 countries.
Countries holding a registration under ATC N02CD03 (fremanezumab), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 10 of them publish a price we can compare per daily dose
Fremanezumab · ATC N02CD03
15 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- FREMANEZUMAB
- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Country
- United States (US)
- ATC code
- N02CD03
- ATC class
- Fremanezumab
- Defined daily dose
- 7.5 mg, P
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 3
- ndc1151759-202-10
- ndc1151759-202-11
- ndc1151759-202-22
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fremanezumab in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaAJOVYTeva GmbH, Ulm
- SwitzerlandAjovy
- FinlandAJOVYTeva GmbH
- United KingdomAjovy 225mg/1.5ml solution for injection pre-filled pensTeva UK Ltd
- BelgiumAjovy 225 mgTeva
- CanadaAJOVYTEVA CANADA LIMITED
- SpainAJOVY 225 MG SOLUCION INYECTABLE EN JERINGA PRECARGADATeva Gmbh
- NetherlandsAJOVY 225 mg, oplossing voor injectie in voorgevulde penTeva GmbH
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Ajovy
- Iceland · Ajovy
- Liechtenstein · Ajovy
- Norway · Ajovy
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/4a8beff8-8ded-4430-a1b0-29bc8512ee7c GET /v1/drugs/4a8beff8-8ded-4430-a1b0-29bc8512ee7c?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": "SUBCUTANEOUS",
"source": "ndc",
"strength": "225",
"substance": "FREMANEZUMAB",
"productndc": "51759-202",
"dosage_form": "INJECTION",
"dea_schedule": null,
"strength_unit": "mg/1.5mL",
"application_number": "BLA761089",
"marketing_category": "BLA"
}See everything about fremanezumab.
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.