United States· US:10122-121_382f1a69-9557-4aeb-b703-6d752c0e786c
Trimbow
A medicinal product containing beclomethasone dipropionate; formoterol fumarate; glycopyrrolate, registered in United States by Chiesi USA, 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
- BECLOMETHASONE DIPROPIONATE; FORMOTEROL FUMARATE; GLYCOPYRROLATE
- Manufacturer
- Chiesi USA, Inc.
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- August 2, 2026
Packs & prices · 1
- ndc1110122-121-02
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Beclomethasone dipropionate; formoterol fumarate; glycopyrrolate in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaTRIMBOWChiesi Farmaceutici S.p.A., Parma
- FinlandRiarifyChiesi Farmaceutici S.p.A.
- IrelandTrimbowChiesi Farmaceutici S.p.A.
- SwedenTrimbow 172 mikrogram/5 mikrogram/9 mikrogram Inhalationsspray, lösningChiesi Farmaceutici S.p.A.
- United KingdomTrimbow 172micrograms/dose / 5micrograms/dose / 9micrograms/dose inhalerChiesi Ltd
- NorwayTrimbowChiesi Farmaceutici S.p.a.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Trimbow, Trydonis
- Liechtenstein · Trimbow, Trydonis
- Norway · Trimbow, Trydonis
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/d1c2e058-b95c-47ba-9d0e-196d104f0b7a GET /v1/drugs/d1c2e058-b95c-47ba-9d0e-196d104f0b7a?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": "200; 6; 12.5",
"substance": "BECLOMETHASONE DIPROPIONATE; FORMOTEROL FUMARATE; GLYCOPYRROLATE",
"productndc": "10122-121",
"dosage_form": "AEROSOL",
"dea_schedule": null,
"strength_unit": "ug/1; ug/1; ug/1",
"application_number": "NDA219622",
"marketing_category": "NDA"
}See everything about beclomethasone dipropionate; formoterol fumarate; glycopyrrolate.
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.