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United States· US:65219-052_935c5395-1f0b-4277-97de-8b1cf1252d1e

Potassium Phosphates

A medicinal product containing monobasic potassium phosphate; dibasic potassium phosphate, registered in United States by Fresenius Kabi USA, LLC.

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…normalisedPotassium PhosphatesATC—REGISTER NO.US:65219-052_935c5395…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MONOBASIC POTASSIUM PHOSPHATE; DIBASIC POTASSIUM PHOSPHATE
Manufacturer
Fresenius Kabi USA, LLC
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
    65219-052-29
  • ndc11
    6521905229
    25 VIAL, SINGLE-DOSE in 1 TRAY (65219-052-29) / 5 mL in 1 VIAL, SINGLE-DOSE (65219-052-09)

Regulatory notes

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

Same medicine, other countries

Monobasic potassium phosphate; dibasic potassium phosphate in 4 other countries

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

All monobasic potassium phosphate; dibasic potassium phosphate products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • Belgium · Kaliphos, Kaliumfosfaat B. Braun
  • Germany · Kaliumphosphat B. Braun
  • Ireland · Potassium Phosphate B Braun Medical
  • Italy · Potassio Fosfato Bioindustria L.I.M., Potassio Fosfato Galenica Senese

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/d614637d-d377-4e18-a9a5-2ec932d5de04
GET /v1/drugs/d614637d-d377-4e18-a9a5-2ec932d5de04?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": "224; 236",
  "substance": "MONOBASIC POTASSIUM PHOSPHATE; DIBASIC POTASSIUM PHOSPHATE",
  "productndc": "65219-052",
  "dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
  "dea_schedule": null,
  "strength_unit": "mg/mL; mg/mL",
  "application_number": "NDA212832",
  "marketing_category": "NDA"
}

See everything about monobasic potassium phosphate; 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.