United States· US:62756-370_99595af6-8c5d-4dc7-8396-e7bce050bb3f
Metoprolol Tartrate and Hydrochlorothiazide
A medicinal product containing metoprolol tartrate; hydrochlorothiazide, registered in United States by Sun Pharmaceutical Industries, 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
- METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE
- Manufacturer
- Sun Pharmaceutical Industries, 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 · 8
- ndc1162756-370-08
- ndc1162756-370-18
- ndc1162756-370-83
- ndc1162756-370-88
- ndc116275637008100 TABLET in 1 BOTTLE (62756-370-08)
- ndc1162756370181000 TABLET in 1 BOTTLE (62756-370-18)
- ndc11627563708330 TABLET in 1 BOTTLE (62756-370-83)
- ndc116275637088100 TABLET in 1 BOTTLE (62756-370-88)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Metoprolol tartrate; hydrochlorothiazide in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyMetodura CompMylan Germany Gmbh
- FinlandHydrosuc CompJacobsen Pharma AS
- United KingdomCo-Betaloc SA tabletsPfizer Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Austria · Metoprolol Ratiopharm
- Germany · Metodura Comp, Metohexal
- Netherlands · Metoprololsuccinaat/Hydrochloorthiazide Sandoz
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/c68600d0-0ad0-4b86-8797-bc2fbe564167 GET /v1/drugs/c68600d0-0ad0-4b86-8797-bc2fbe564167?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": "50; 25",
"substance": "METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE",
"productndc": "62756-370",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1",
"application_number": "ANDA090654",
"marketing_category": "ANDA"
}See everything about metoprolol tartrate; 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.