United States· US:0069-0235_d85989f4-41dc-4e3a-a0fa-759b68e1130c
Cibinqo
A medicinal product containing abrocitinib, registered in United States by Pfizer Laboratories Div Pfizer 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
- abrocitinib
- Manufacturer
- Pfizer Laboratories Div Pfizer 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 12, 2026
Packs & prices · 1
- ndc11006902353030 TABLET, FILM COATED in 1 BOTTLE (0069-0235-30)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Abrocitinib in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaCIBINQOPfizer Europe MA EEIG, Bruxelles
- SwitzerlandCibinqo
- FranceCIBINQO 50 mg, comprimé pelliculéPFIZER EUROPE MA EEIG (BELGIQUE)
- BelgiumCibinqo 50 mgPfizer Europe MA
- IcelandCibinqoPfizer Europe MA EEIG*
- NetherlandsCibinqo 50 mg, filmomhulde tablettenPfizer Europe MA EEIG
- NorwayCibinqoPfizer Europe MA EEIG
- PolandCibinqoPfizer Europe MA EEIG
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Cibinqo
- Liechtenstein · Cibinqo
- Norway · Cibinqo
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/e0ed93de-179f-4c35-a3db-488d809070e2 GET /v1/drugs/e0ed93de-179f-4c35-a3db-488d809070e2?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",
"livertox": {
"summary": null,
"livertox_id": null,
"hepatotoxicity_score": 5
},
"productid": "0069-0235_d85989f4-41dc-4e3a-a0fa-759b68e1130c",
"productndc": "0069-0235",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ABROCITINIB",
"proprietary_name": "Cibinqo",
"active_ingred_unit": "mg/1",
"application_number": "NDA213871",
"marketing_category": "NDA",
"nonproprietary_name": "abrocitinib",
"start_marketing_date": "20220224",
"active_numerator_strength": "50"
}See everything about abrocitinib.
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.