United States· US:73302-456_30e0d760-1e27-456f-8420-ad1c219f49f7
Ella
A medicinal product containing ulipristal acetate, registered in United States by PMI Branded Pharmaceuticals, Inc..
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
- ULIPRISTAL ACETATE
- Manufacturer
- PMI Branded Pharmaceuticals, Inc.
- 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 · 1
- ndc1173302-456-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ulipristal acetate in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomEllaOne 30mg tabletsEthigen Ltd
- FinlandellaOneParanova Oy
- CzechiaELLAONELaboratoire HRA Pharma, Chatillon
- NetherlandsellaOne, 30 mg tablettenLaboratoire HRA Pharma
- PolandellaOneLaboratoire HRA Pharma
- SwedenellaOne 30 mg TablettLaboratoire HRA Pharma
- IrelandellaOne 30 mg tabletLaboratoire HRA Pharma
- SpainELLAONE 30 mg COMPRIMIDOSLaboratoire Hra Pharma
Authorised across Europe · EMA
The same active substance is authorised in 19 EEA countries. Names it is sold under:
- Austria · Lencya, Ulipristal Acetate Hexal
- Czechia · Ulipristal Acetate Aristo
- Germany · Femke, Lencya
- Denmark · Femke, Ulipristal Acetate Stada
- Spain · Ulipristal Aristo, Ulipristal Aurovitas
- Finland · Femke, Ulipristal Acetate Stada
- France · Ulipristal Acetate Biogaran, Ulipristal Acétate Exeltis
- United Kingdom (Northern Ireland) · Contrella, Ellaone
- Greece · Boled, Elperil
- Ireland · Ulipristal Acetate Rowex
- Iceland · Ellaone, Ulipristal Acetate Stada
- Italy · Evante, Lencya
- Liechtenstein · Ellaone
- Malta · Ecinq
- Netherlands · Ecinq, Evante
- Norway · Ellaone, Femke
- Poland · Misstala, Ulipristal Aristo
- Portugal · Femke, Ulipristal Aristo
- Sweden · Ulipristal Acetate Stada
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/a3b78d0d-4125-4793-8208-5ad349df29c7 GET /v1/drugs/a3b78d0d-4125-4793-8208-5ad349df29c7?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": "ORAL",
"source": "ndc",
"strength": "30",
"substance": "ULIPRISTAL ACETATE",
"productndc": "73302-456",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "NDA022474",
"marketing_category": "NDA"
}See everything about ulipristal acetate.
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.