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United States· US:69097-972_25e66ad5-947a-4262-a996-a9695601d301

Fosinopril Sodium and Hydrochlorothiazide

A medicinal product containing fosinopril sodium; hydrochlorothiazide, registered in United States by CIPLA USA INC..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedFosinopril Sodium and Hydrochlorothia…ATC—REGISTER NO.US:69097-972_25e66ad5…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Manufacturer
CIPLA 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
September 27, 2026

Packs & prices · 2

  • ndc11
    6909797207
    100 TABLET in 1 BOTTLE (69097-972-07)
  • ndc11
    69097-972-07

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Fosinopril sodium; hydrochlorothiazide in 4 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All fosinopril sodium; hydrochlorothiazide products

Authorised across Europe · EMA

The same active substance is authorised in 15 EEA countries. Names it is sold under:

  • Austria · Fosicomb, Fosinopril-Natrium/Hct Actavis
  • Bulgaria · Монозид
  • Czechia · Monace Combi
  • Estonia · Fosinopril Hct Actavis
  • Spain · Fositens Plus
  • France · Fosinopril Hydrochlorothiazide Arrow, Fosinopril/Hydrochlorothiazide Arrow Lab
  • Hungary · Duopril, Fosicard Plus
  • Italy · Fosicombi, Fosinopril E Idroclorotiazide Doc Generici
  • Lithuania · Fosinopril Hct Actavis
  • Latvia · Fosinopril Hct Actavis
  • Malta · Fosinopril + Hydrochlorothiazide Aurobindo
  • Netherlands · Fosinoprilnatrium/Hydrochloorthiazide Aurobindo
  • Portugal · Fosinopril + Hidroclorotiazida Aurobindo, Fosinopril + Hidroclorotiazida Aurovitas
  • Slovenia · Monopril Plus
  • Slovakia · Monozide

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/218bd4c1-d356-4d14-9275-f2d8b04ee6d4
GET /v1/drugs/218bd4c1-d356-4d14-9275-f2d8b04ee6d4?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": "10; 12.5",
  "substance": "FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE",
  "productndc": "69097-972",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1",
  "application_number": "ANDA090228",
  "marketing_category": "ANDA"
}

See everything about fosinopril sodium; 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.