Home › NDC Lookup › RxCUI directory › RxCUI 212218

Epoetin alfa 20000 UNT/ML Injectable Solution [Epogen] — RxCUI 212218

RxNorm drug concept · Semantic branded drug
RxCUI 212218 Semantic branded drug · SBD ● Current RxNorm concept 6 FDA products 12 package NDCs Snapshot Jul 14, 2026

This page is curated, coded, and maintained by

Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI212218
Official nameEpoetin alfa 20000 UNT/ML Injectable Solution [Epogen]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asEpogen 20000 UNT/ML Injectable Solution; EPOGEN 20,000 UNT/ML Injectable Solution; EPO 20000 UNT/ML Injectable Solution [Epogen]; Epogen (epoetin alfa 20,000 UNT/ML) Injectable Solution; ERYTHROPOIETIN 20000 UNT/ML Injectable Solution [Epogen]
FDA products mapped6
Package NDCs mapped12
Reported Medicaid activity (SDUD)200,629 prescriptions · 31 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

🕸️ Concept Web — How Epoetin alfa 20000 UNT/ML Injectable Solution [E... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Epoetin alfa 20000 UNT/ML Injectable Solution [Epogen] RxCUI 212218

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 1

    The active substance itself — no strength, form, or brand attached yet.

    • Epoetin alfa 105694
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Epogen 203281
  3. Dose forms 6

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Epoetin alfa Injectable Solution 372032
    • Epoetin alfa Injectable Product 1163895
    • Epoetin alfa Injectable Solution [Epogen] 92613
    • Epogen Injectable Product 1167637
    • Injectable Solution 316949
    • Injectable Product 1151126
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 11 of 11 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

Brand-Name Concepts

  • Epoetin alfa 20000 UNT/ML [Epogen] SBDC · 572441
  • Epoetin alfa Injectable Solution [Epogen] SBDF · 92613
  • Epogen Injectable Product SBDG · 1167637
  • Epogen BN · 203281

📦 FDA Products & Package NDCs

6 products · 12 package NDCs
12 package NDCs map to RxCUI 212218 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
55513-0126-10 10 VIAL in 1 PACKAGE (55513-126-10) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1989-06-30
55513-0126-20 10 VIAL in 1 PACKAGE (55513-126-20) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
55513-0144-10 10 VIAL in 1 PACKAGE (55513-144-10) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1993-08-16
55513-0144-20 10 VIAL in 1 PACKAGE (55513-144-20) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
55513-0148-10 10 VIAL in 1 PACKAGE (55513-148-10) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1993-08-16
55513-0148-20 10 VIAL in 1 PACKAGE (55513-148-20) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
55513-0267-10 10 VIAL in 1 PACKAGE (55513-267-10) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1990-04-30
55513-0267-20 10 VIAL in 1 PACKAGE (55513-267-20) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
55513-0283-10 10 VIAL in 1 PACKAGE (55513-283-10) / 2 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1994-12-05
55513-0283-20 10 VIAL in 1 PACKAGE (55513-283-20) / 2 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
55513-0478-10 10 VIAL in 1 PACKAGE (55513-478-10) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 1997-03-03
55513-0478-20 10 VIAL in 1 PACKAGE (55513-478-20) / 1 mL in 1 VIAL (55513... EPOGEN Amgen, Inc 2025-04-14
Observed labelers: Amgen, Inc (12) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🧾 Billing Codes (HCPCS)

Medical billing codes (HCPCS "J-codes") that connect to this concept's packages — used mostly when a clinic or hospital bills for a drug it administers. Each code links to its full billing page.
CodeDescriptorMapped packagesSources
J0885 Epoetin alfa, non-esrd 8 CMS
Q4081 Epoetin alfa, 100 units esrd 8 CMS
⚠ A crosswalk is not coverage: an NDC↔HCPCS mapping does not guarantee any payer covers or pays the code. Always verify the current payer policy before billing.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.