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United States· US:37662-1736_eb6ac6ad-4678-1072-e053-2995a90a02e9

Kali Phosphoricum

A medicinal product containing dibasic potassium phosphate, 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 PhosphoricumATC—REGISTER NO.US:37662-1736_eb6ac6a…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DIBASIC POTASSIUM PHOSPHATE
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
    3766217361
    200 PELLET in 1 VIAL, GLASS (37662-1736-1)
  • ndc11
    3766217362
    500 PELLET in 1 VIAL, GLASS (37662-1736-2)
  • ndc11
    3766217363
    3000 PELLET in 1 BOTTLE, GLASS (37662-1736-3)
  • ndc11
    3766217364
    10000 PELLET in 1 BOTTLE, GLASS (37662-1736-4)
  • ndc11
    37662-1736-1
  • ndc11
    37662-1736-2
  • ndc11
    37662-1736-3
  • ndc11
    37662-1736-4

Regulatory notes

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

Same medicine, other countries

Dibasic potassium phosphate in 3 other countries

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

All dibasic potassium phosphate products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Spain · Fosfato Dipotasico 1m Fresenius Kabi
  • France · Phosphate Dipotassique Renaudin

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/c02e5484-59bd-458a-83d8-113f66d8b5d8
GET /v1/drugs/c02e5484-59bd-458a-83d8-113f66d8b5d8?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": "200",
  "substance": "DIBASIC POTASSIUM PHOSPHATE",
  "productndc": "37662-1736",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about dibasic potassium phosphate.

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.