United States· US:37662-1473_e81be440-31a4-53e1-e053-2995a90ace9e

Kali Bichromicum

A medicinal product containing potassium dichromate, registered in United States by Hahnemann Laboratories, 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…normalisedKali BichromicumATC—REGISTER NO.US:37662-1473_e81be44…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
POTASSIUM DICHROMATE
Manufacturer
Hahnemann Laboratories, 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

  • ndc11
    37662-1473-1
  • ndc11
    37662-1473-2
  • ndc11
    37662-1473-3
  • ndc11
    37662-1473-4
  • ndc11
    3766214731
    200 PELLET in 1 VIAL, GLASS (37662-1473-1)
  • ndc11
    3766214732
    500 PELLET in 1 VIAL, GLASS (37662-1473-2)
  • ndc11
    3766214733
    3000 PELLET in 1 BOTTLE, GLASS (37662-1473-3)
  • ndc11
    3766214734
    10000 PELLET in 1 BOTTLE, GLASS (37662-1473-4)

Regulatory notes

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

Same medicine, other countries

Potassium dichromate in 1 other country

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

All potassium dichromate products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Germany · Kaliumdichromat Smartpractice Europe

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/fdce0abe-61cd-472f-9e6a-f3b9850674b0
GET /v1/drugs/fdce0abe-61cd-472f-9e6a-f3b9850674b0?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",
  "substance": "POTASSIUM DICHROMATE",
  "productndc": "37662-1473",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about potassium dichromate.

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.