United States· US:70710-1876_245bc553-262e-47ff-91d0-0b7c136b6413
zinc sulfate
A medicinal product containing zinc sulfate, registered in United States by Zydus Pharmaceuticals USA 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
- ZINC SULFATE
- Manufacturer
- Zydus Pharmaceuticals 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
- ndc11707101876725 VIAL in 1 CARTON (70710-1876-7) / 10 mL in 1 VIAL (70710-1876-1)
- ndc1170710-1876-7
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Zinc sulfate in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomAactizinc 125mg effervescent tabletsTriOn Pharma Ltd
- FinlandOftan-ZinkSanten Oy
- BelgiumZincfrin 2.5 mg/ml - 1.2 mg/mlNovartis Pharma
- NorwaySolvezinkKaro Pharma AB (1)
- PolandZincteralTeva Pharmaceuticals Polska Sp. z o.o.
- SwedenSolvezink 45 mg Zn 2+ BrustablettKaro Pharma AB
- Japan硫酸亜鉛水和物
- SwitzerlandVirudermin, Gelsteinberg pharma ag
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Zinc Sulfate
- Norway · Solvezink
- Sweden · Solvezink
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/ddfe8a98-35b4-4be4-bf85-4030ba4c47ec GET /v1/drugs/ddfe8a98-35b4-4be4-bf85-4030ba4c47ec?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": "INTRAVENOUS",
"source": "ndc",
"strength": "1",
"substance": "ZINC SULFATE",
"productndc": "70710-1876",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA217074",
"marketing_category": "ANDA"
}See everything about zinc sulfate.
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.