United States· US:0574-0229_55072852-c532-448e-935e-102e981cf698
benazepril hydrochloride and hydrochlorothiazide
A medicinal product containing benazepril hydrochloride; hydrochlorothiazide, registered in United States by Padagis US LLC.
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
- BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- Manufacturer
- Padagis US LLC
- 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 · 2
- ndc110574022901100 TABLET in 1 BOTTLE (0574-0229-01)
- ndc110574-0229-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Benazepril hydrochloride; hydrochlorothiazide in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyBenazeplusStadapharm Gmbh
- FranceBENAZEPRIL HYDROCHLOROTHIAZIDE EG 10 mg/12,5 mg, comprimé pelliculé sécableEG LABO - LABORATOIRES EUROGENERICS
- ItalyBENAZEPRIL IDROCLOROTIAZIDE EGEG S.P.A.
- SpainCIBADREX 10 mg / 12,5 mg COMPRIMIDOS RECUBIERTOS CON PELICULAMeda Pharma S.L.
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Germany · Benazeplus, Benazepril Comp 1 A Pharma
- France · Benazepril Hydrochlorothiazide Eg, Benazepril/Hydrochlorothiazide Arrow
- Greece · Cibadrex
- Hungary · Lotensin Hct
- Italy · Benazepril Idroclorotiazide Eg, Benazepril Idroclorotiazide Sandoz
- Netherlands · Benazepril Hcl/Hydrochloorthiazide Hexal Ag
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/a6b55f27-efc7-4569-9915-6f47fa12a648 GET /v1/drugs/a6b55f27-efc7-4569-9915-6f47fa12a648?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": "20; 12.5",
"substance": "BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE",
"productndc": "0574-0229",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1",
"application_number": "NDA020033",
"marketing_category": "NDA AUTHORIZED GENERIC"
}See everything about benazepril hydrochloride; hydrochlorothiazide.
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.