United States· US:33342-295_94a44831-98b3-41d4-89da-89a43b25d15f
Fenofibric acid
A choline fenofibrate product containing choline fenofibrate, registered in United States by Macleods Pharmaceuticals Limited. The same ATC class is registered in 2 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Choline fenofibrate is registered in 2 of 19 countries.
Countries holding a registration under ATC C10AB11 (choline fenofibrate), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 2 of them publish a price we can compare per daily dose
Choline fenofibrate · ATC C10AB11
2 / 19 countries
- Switzerlandprice
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- CHOLINE FENOFIBRATE
- Manufacturer
- Macleods Pharmaceuticals Limited
- Country
- United States (US)
- ATC code
- C10AB11
- ATC class
- Choline fenofibrate
- Defined daily dose
- 0.135 g, O
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 4
- ndc11333422951090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-295-10)
- ndc11333422955610 BLISTER PACK in 1 CARTON (33342-295-56) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
- ndc1133342-295-10
- ndc1133342-295-56
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under C10AB11
Choline fenofibrate, as other registers publish it.
- United StatesFenofibric acidLupin Pharmaceuticals, Inc.
- United StatesFenofibric acidMacleods Pharmaceuticals Limited
- United StatesFenofibric acidLupin Pharmaceuticals, Inc.
- SwitzerlandTrilipix 135 mg, Hartkapseln, retardiertViatris Pharma GmbH
- SwitzerlandTrilipix 45 mg, Hartkapseln, retardiertViatris Pharma GmbH
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/b0ab1974-2df0-497a-b076-20e30c10e8ec GET /v1/drugs/b0ab1974-2df0-497a-b076-20e30c10e8ec?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": "135",
"substance": "CHOLINE FENOFIBRATE",
"productndc": "33342-295",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "ANDA207796",
"marketing_category": "ANDA"
}See everything about choline fenofibrate.
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.