United States· US:68083-608_cfa59996-1de2-4313-a7ac-1766764513e2

Zinc Sulfate

A medicinal product containing zinc sulfate, registered in United States by Gland Pharma Limited.

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…normalisedZinc SulfateATC—REGISTER NO.US:68083-608_cfa59996…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ZINC SULFATE
Manufacturer
Gland Pharma 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 · 2

  • ndc11
    68083-608-25
  • ndc11
    6808360825
    25 VIAL in 1 CARTON (68083-608-25) / 10 mL in 1 VIAL

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.

All zinc sulfate products

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/d4413002-13a9-4ee5-a4da-8a96c0971ad8
GET /v1/drugs/d4413002-13a9-4ee5-a4da-8a96c0971ad8?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": "68083-608",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA216249",
  "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.