United States· US:70771-1362_1b1be913-613c-469c-8665-13858922d5bf
triamterene and hydrochlorothiazide
A medicinal product containing triamterene; hydrochlorothiazide, registered in United States by Zydus Lifesciences Limited.
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
- TRIAMTERENE; HYDROCHLOROTHIAZIDE
- Manufacturer
- Zydus Lifesciences Limited
- 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 · 8
- ndc1170771136201000 TABLET in 1 BOTTLE (70771-1362-0)
- ndc117077113621100 TABLET in 1 BOTTLE (70771-1362-1)
- ndc11707711362410 BLISTER PACK in 1 CARTON (70771-1362-4) / 10 TABLET in 1 BLISTER PACK
- ndc117077113625500 TABLET in 1 BOTTLE (70771-1362-5)
- ndc1170771-1362-0
- ndc1170771-1362-1
- ndc1170771-1362-4
- ndc1170771-1362-5
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Triamterene; hydrochlorothiazide in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyDytide HMibe Gmbh Arzneimittel
- CanadaAPO TRIAZIDEAPOTEX INC
- FinlandTriamtexOrion Corporation Orion Pharma
- FrancePRESTOLE, géluleALMIRALL
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Austria · Dytide H
- Bulgaria · Диуретидин, Триампур Композитум
- Germany · Dytide H, Triampur Compositum
- France · Prestole
- Netherlands · Triamtereen/Hydrochloorthiazide Accord
- Portugal · Dyazide
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/e53abe13-fd70-4042-bb32-b26de7392d3a GET /v1/drugs/e53abe13-fd70-4042-bb32-b26de7392d3a?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": "75; 50",
"substance": "TRIAMTERENE; HYDROCHLOROTHIAZIDE",
"productndc": "70771-1362",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1",
"application_number": "ANDA208360",
"marketing_category": "ANDA"
}See everything about triamterene; 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.