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2 ML anifrolumab-fnia 150 MG/ML Injection — RxCUI 2565280

RxNorm drug concept · Semantic clinical drug
RxCUI 2565280 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 4 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

RxCUI2565280
Official name2 ML anifrolumab-fnia 150 MG/ML Injection
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asanifrolumab-fnia 300 MG per 2 ML Injection; anifrolumab-fnia 300 MG in 2 ML Injection
FDA products mapped2
Package NDCs mapped4
Reported Medicaid activity (SDUD)10,185 prescriptions · 39 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Anifrolumab-fnia Injection: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
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  • What exactly is Saphnelo and why has my doctor prescribed it for my lupus?
  • There are two options. One is an IV infusion given at a clinic or infusion center by a healthcare provider, once every four weeks — each session takes about 30 minutes. The other i...
  • How will I actually receive this medication — will I have to go to a clinic every time?
📖 Read our full Anifrolumab-fnia Injection guide →

🕸️ Concept Web — How 2 ML anifrolumab-fnia 150 MG/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 2 ML anifrolumab-fnia 150 MG/ML Injection RxCUI 2565280

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

  1. Ingredients 2

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

    • Anifrolumab 2565265
    • Anifrolumab-fnia 2565276
  2. Brand names 1

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

    • Saphnelo 2565282
  3. Dose forms 9

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

    • Anifrolumab Injection 2565279
    • Anifrolumab-fnia Injection 2648738
    • Anifrolumab Injectable Product 2565278
    • Anifrolumab-fnia Injectable Product 2662358
    • Anifrolumab Injection [Saphnelo] 2565285
    • Anifrolumab-fnia Injection [Saphnelo] 2654925
    • Saphnelo Injectable Product 2565284
    • Injection 1649574
    • +1 more in this family
  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 — 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

  • Anifrolumab-fnia 150 MG/ML SCDC · 2565277
  • Anifrolumab Injection SCDF · 2565279
  • Anifrolumab-fnia Injection SCDFP · 2648738
  • Anifrolumab Injectable Product SCDG · 2565278
  • Anifrolumab-fnia Injectable Product SCDGP · 2662358

Brand-Name Concepts

  • 2 ML anifrolumab-fnia 150 MG/ML Injection [Saphnelo] SBD · 2565286
  • Anifrolumab-fnia 150 MG/ML [Saphnelo] SBDC · 2565283
  • Anifrolumab Injection [Saphnelo] SBDF · 2565285
  • Anifrolumab-fnia Injection [Saphnelo] SBDFP · 2654925
  • Saphnelo Injectable Product SBDG · 2565284
  • Saphnelo BN · 2565282

📦 FDA Products & Package NDCs

2 products · 4 package NDCs
4 package NDCs map to RxCUI 2565280 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
00310-3040-00 1 VIAL, GLASS in 1 CARTON (0310-3040-00) / 2 mL in 1 VIAL,... SAPHNELO AstraZeneca Pharmaceuticals LP 2021-07-30
00310-3080-01 1 SYRINGE, GLASS in 1 CARTON (0310-3080-01) / .8 mL in 1 SY... SAPHNELO AstraZeneca Pharmaceuticals LP 2026-04-24
00310-3080-02 1 SYRINGE, GLASS in 1 CARTON (0310-3080-02) / .8 mL in 1 SY... SAPHNELO AstraZeneca Pharmaceuticals LP 2026-04-24
00310-3080-95 1 SYRINGE, GLASS in 1 CARTON (0310-3080-95) / .8 mL in 1 SY... SAPHNELO AstraZeneca Pharmaceuticals LP 2026-04-24
Observed labelers: AstraZeneca Pharmaceuticals LP (4) — 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
J0491 Inj anifrolumab-fnia 1mg 1 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.