United States· US:55513-148_79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd

EPOGEN

A medicinal product containing epoetin, registered in United States by Amgen, 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…normalisedEPOGENATC—REGISTER NO.US:55513-148_79ccf986…PACKS LISTED4CHECKEDJune 26, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
EPOETIN
Manufacturer
Amgen, Inc
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 26, 2026

Packs & prices · 4

  • ndc11
    5551314810
    10 VIAL in 1 PACKAGE (55513-148-10) / 1 mL in 1 VIAL (55513-148-01)
  • ndc11
    5551314820
    10 VIAL in 1 PACKAGE (55513-148-20) / 1 mL in 1 VIAL (55513-148-01)
  • ndc11
    55513-148-10
  • ndc11
    55513-148-20

Regulatory notes

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

Same medicine, other countries

Epoetin in 17 other countries

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

All epoetin products

Authorised across Europe · EMA

The same active substance is authorised in 16 EEA countries. Names it is sold under:

  • Austria · Erypo
  • Belgium · Eprex
  • Czechia · Eprex
  • Germany · Erypo Fs
  • Spain · Eprex
  • France · Eprex
  • United Kingdom (Northern Ireland) · Eprex
  • Greece · Eprex
  • Iceland · Abseamed, Binocrit
  • Italy · Eprex
  • Liechtenstein · Binocrit, Epoetin Alfa Hexal
  • Luxembourg · Eprex
  • Netherlands · Eprex
  • Norway · Abseamed, Binocrit
  • Portugal · Eprex
  • Slovenia · Eprex

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/fc5abd1c-dabc-44d6-9393-a26805e0503b
GET /v1/drugs/fc5abd1c-dabc-44d6-9393-a26805e0503b?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; SUBCUTANEOUS",
  "source": "ndc",
  "strength": "4000",
  "substance": "EPOETIN",
  "productndc": "55513-148",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "strength_unit": "[iU]/mL",
  "application_number": "BLA103234",
  "marketing_category": "BLA"
}

See everything about epoetin.

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.