1 ML epoetin alfa-epbx 40000 UNT/ML Injection — RxCUI 2047621
RxNorm drug concept · Semantic clinical drug
RxCUI 2047621
Semantic clinical drug · SCD
● Current RxNorm concept 7 FDA products
7 package NDCs
Snapshot Jul 14, 2026
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
RxCUI2047621
Official name1 ML epoetin alfa-epbx 40000 UNT/ML Injection
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known as1 ML EPO-epbx 40000 UNT/ML Injection; epoetin alfa-epbx 40,000 UNT in 1 ML Injection; 1 ML ERYTHROPOIETIN-epbx 40000 UNT/ML Injection; epoetin alfa-epbx 40,000 UNT per 1 ML Injection
FDA products mapped7
Package NDCs mapped7
Reported Medicaid activity (SDUD)24,911 prescriptions · 43 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
🕸️ Concept Web — How 1 ML epoetin alfa-epbx 40000 UNT/ML Injection 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
1 ML epoetin alfa-epbx 40000 UNT/ML Injection
RxCUI 2047621 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
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Epoetin alfa
105694IN -
Epoetin alfa-epbx
2047589PIN
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Epoetin alfa
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Retacrit
2047592BN
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Retacrit
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Epoetin alfa Injection
1721637SCDF -
Epoetin alfa-epbx Injection
2646640SCDFP -
Epoetin alfa Injectable Product
1163895SCDG -
Epoetin alfa-epbx Injectable Product
2660947SCDGP -
Epoetin alfa Injection [Retacrit]
2047594SBDF -
Epoetin alfa-epbx Injection [Retacrit]
2657314SBDFP -
Retacrit Injectable Product
2047595SBDG -
Injection
1649574DF - +1 more in this family
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Epoetin alfa Injection
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Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Epoetin alfa-epbx 40000 UNT/ML
2047620SCDC -
1 ML epoetin alfa-epbx 40000 UNT/ML Injection [Retacrit]
2047623SBD -
Epoetin alfa-epbx 40000 UNT/ML [Retacrit]
2047622SBDC
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Epoetin alfa-epbx 40000 UNT/ML
Showing up to 8 concepts per family — 14 of 15 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
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Epoetin alfa-epbx 40000 UNT/ML
SCDC · 2047620 -
Epoetin alfa Injection
SCDF · 1721637 -
Epoetin alfa-epbx Injection
SCDFP · 2646640 -
Epoetin alfa Injectable Product
SCDG · 1163895 -
Epoetin alfa-epbx Injectable Product
SCDGP · 2660947
Brand-Name Concepts
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1 ML epoetin alfa-epbx 40000 UNT/ML Injection [Retacrit]
SBD · 2047623 -
Epoetin alfa-epbx 40000 UNT/ML [Retacrit]
SBDC · 2047622 -
Epoetin alfa Injection [Retacrit]
SBDF · 2047594 -
Epoetin alfa-epbx Injection [Retacrit]
SBDFP · 2657314 -
Retacrit Injectable Product
SBDG · 2047595 -
Retacrit
BN · 2047592
📦 FDA Products & Package NDCs
7 products · 7 package NDCs
7 package NDCs map to RxCUI 2047621 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 |
|---|---|---|---|---|
| 00069-1305-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1305-10) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2018-06-18 |
| 00069-1306-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1306-10) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2018-06-18 |
| 00069-1307-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1307-10) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2018-06-18 |
| 00069-1308-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1308-10) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2018-06-18 |
| 00069-1309-04 | 4 VIAL, SINGLE-DOSE in 1 CARTON (0069-1309-04) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2018-06-18 |
| 00069-1311-10 | 10 VIAL, MULTI-DOSE in 1 CARTON (0069-1311-10) / 1 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2020-11-09 |
| 00069-1318-10 | 10 VIAL, MULTI-DOSE in 1 CARTON (0069-1318-10) / 2 mL in 1... | RETACRIT | Pfizer Laboratories Div Pfizer Inc | 2020-11-09 |
Observed labelers:
Pfizer Laboratories Div Pfizer Inc (7)
— 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.
| Code | Descriptor | Mapped packages | Sources |
|---|---|---|---|
| Q5105 | Inj retacrit esrd on dialysi | 7 | CMS |
| Q5106 | Inj retacrit non-esrd use | 7 | 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.