United States· US:59088-171_f204b4b3-176f-8839-e053-2a95a90a7115

Vitranol

A medicinal product containing pyridoxine hydrochloride; selenium; folic acid; magnesium oxide; molybdenum; thiamine mononitrate; cyanocobalamin; vitamin a acetate; chromium nicotinate; cholecalciferol; riboflavin; niacinamide; .alpha.-tocopherol acetate, dl-; zinc oxide; calcium carbonate; ascorbic acid; manganese sulfate, registered in United States by PureTek Corporation.

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedVitranolATC—REGISTER NO.US:59088-171_f204b4b3…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PYRIDOXINE HYDROCHLORIDE; SELENIUM; FOLIC ACID; MAGNESIUM OXIDE; MOLYBDENUM; THIAMINE MONONITRATE; CYANOCOBALAMIN; VITAMIN A ACETATE; CHROMIUM NICOTINATE; CHOLECALCIFEROL; RIBOFLAVIN; NIACINAMIDE; .ALPHA.-TOCOPHEROL ACETATE, DL-; ZINC OXIDE; CALCIUM CARBONATE; ASCORBIC ACID; MANGANESE SULFATE
Manufacturer
PureTek Corporation
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
    59088-171-54
  • ndc11
    5908817154
    30 TABLET in 1 BOTTLE, PLASTIC (59088-171-54)

Regulatory notes

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

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/0e641069-17e9-45c9-9644-204c6dc331de
GET /v1/drugs/0e641069-17e9-45c9-9644-204c6dc331de?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": "20; 55; 1000; 200; 45; 3; 8; 1500; 35; 20; 3.4; 20; 30; 25; 200; 120; 2.3",
  "substance": "PYRIDOXINE HYDROCHLORIDE; SELENIUM; FOLIC ACID; MAGNESIUM OXIDE; MOLYBDENUM; THIAMINE MONONITRATE; CYANOCOBALAMIN; VITAMIN A ACETATE; CHROMIUM NICOTINATE; CHOLECALCIFEROL; RIBOFLAVIN; NIACINAMIDE; .ALPHA.-TOCOPHEROL ACETATE, DL-; ZINC OXIDE; CALCIUM CARBONATE; ASCORBIC ACID; MANGANESE SULFATE",
  "productndc": "59088-171",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about pyridoxine hydrochloride; selenium; folic acid; magnesium oxide; molybdenum; thiamine mononitrate; cyanocobalamin; vitamin a acetate; chromium nicotinate; cholecalciferol; riboflavin; niacinamide; .alpha.-tocopherol acetate, dl-; zinc oxide; calcium carbonate; ascorbic acid; manganese 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.