United States· US:59212-700_d172c0d5-b118-4433-92bd-05214976dd8f

Orapred

A medicinal product containing prednisolone sodium phosphate, registered in United States by Advanz Pharma (US) Corp..

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…normalisedOrapredATC—REGISTER NO.US:59212-700_d172c0d5…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PREDNISOLONE SODIUM PHOSPHATE
Manufacturer
Advanz Pharma (US) Corp.
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
    5921270012
    2 BLISTER PACK in 1 CARTON (59212-700-12) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59212-700-06)
  • ndc11
    59212-700-12

Regulatory notes

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

Same medicine, other countries

Prednisolone sodium phosphate in 7 other countries

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

All prednisolone sodium phosphate products

Authorised across Europe · EMA

The same active substance is authorised in 12 EEA countries. Names it is sold under:

  • Cyprus · Adelone, Prednisolone Bausch+lomb
  • Germany · Okrido
  • Denmark · Prednisolon Unimedic
  • Spain · Prednisolona Minims
  • Finland · Provistopto
  • United Kingdom (Northern Ireland) · Prednisolone Rph Pharmaceuticals, Prednisolone Sodium Phosphate Aspire Pharma
  • Greece · Adelone, Cordeslon
  • Ireland · Minims
  • Malta · Minims, Provist-Opto
  • Netherlands · Minims Prednisolondinatriumfosfaat Bausch Health Ireland, Provist-Opto
  • Norway · Prednisolon Unimedic
  • Sweden · Prednisolon Evolan, Prednisolon Unimedic

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/f9875da5-60df-4fed-b444-2271c081816e
GET /v1/drugs/f9875da5-60df-4fed-b444-2271c081816e?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": "PREDNISOLONE SODIUM PHOSPHATE",
  "productndc": "59212-700",
  "dosage_form": "TABLET, ORALLY DISINTEGRATING",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "NDA021959",
  "marketing_category": "NDA"
}

See everything about prednisolone sodium 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.