1.14 ML sarilumab 132 MG/ML Auto-Injector — RxCUI 2003755
RxNorm drug concept · Semantic clinical drug
RxCUI 2003755
Semantic clinical drug · SCD
● Current RxNorm concept 4 FDA products
8 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
RxCUI2003755
Official name1.14 ML sarilumab 132 MG/ML Auto-Injector
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known assarilumab 150 MG per 1.14 ML Auto-Injector; sarilumab 150 MG in 1.14 ML Auto-Injector
FDA products mapped4
Package NDCs mapped8
Reported Medicaid activity (SDUD)5,765 prescriptions · 35 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 Sarilumab Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Kevzara targets a specific protein called IL-6 that drives inflammation in your joints and body. Unlike traditional DMARDs (like methotrexate), which work more broadly, Kevzara zer...
- What exactly is Kevzara treating — and how is it different from other arthritis medicines?
- You'll use a pre-filled syringe or pre-filled pen, injecting it under the skin — usually in the belly, thigh, or upper arm. Before injecting, let the pre-filled syringe sit at room...
- How do I give myself this injection at home?
🕸️ Concept Web — How 1.14 ML sarilumab 132 MG/ML Auto-Injector 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
1.14 ML sarilumab 132 MG/ML Auto-Injector
RxCUI 2003755 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
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Sarilumab
1923319IN
-
Sarilumab
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Kevzara
1923334BN
-
Kevzara
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Sarilumab Auto-Injector
2003754SCDF -
Sarilumab Injectable Product
1923331SCDG -
Sarilumab Auto-Injector [Kevzara]
2003756SBDF -
Kevzara Injectable Product
1923337SBDG -
Auto-Injector
1649570DF -
Injectable Product
1151126DFG
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Sarilumab Auto-Injector
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Sarilumab 132 MG/ML
1923330SCDC -
1.14 ML sarilumab 132 MG/ML Auto-Injector [Kevzara]
2003757SBD -
Sarilumab 132 MG/ML [Kevzara]
1923335SBDC
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Sarilumab 132 MG/ML
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
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Sarilumab 132 MG/ML
SCDC · 1923330 -
Sarilumab Auto-Injector
SCDF · 2003754 -
Sarilumab Injectable Product
SCDG · 1923331
Brand-Name Concepts
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1.14 ML sarilumab 132 MG/ML Auto-Injector [Kevzara]
SBD · 2003757 -
Sarilumab 132 MG/ML [Kevzara]
SBDC · 1923335 -
Sarilumab Auto-Injector [Kevzara]
SBDF · 2003756 -
Kevzara Injectable Product
SBDG · 1923337 -
Kevzara
BN · 1923334
📦 FDA Products & Package NDCs
4 products · 8 package NDCs
8 package NDCs map to RxCUI 2003755 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 |
|---|---|---|---|---|
| 00024-5908-01 | 2 SYRINGE in 1 PACKAGE (0024-5908-01) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2017-05-22 |
| 00024-5908-02 | 2 SYRINGE in 1 PACKAGE (0024-5908-02) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2017-05-22 |
| 00024-5910-01 | 2 SYRINGE in 1 PACKAGE (0024-5910-01) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2017-05-22 |
| 00024-5910-02 | 2 SYRINGE in 1 PACKAGE (0024-5910-02) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2017-05-22 |
| 00024-5920-01 | 2 SYRINGE in 1 PACKAGE (0024-5920-01) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2018-04-13 |
| 00024-5920-02 | 2 SYRINGE in 1 PACKAGE (0024-5920-02) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2018-04-13 |
| 00024-5922-01 | 2 SYRINGE in 1 PACKAGE (0024-5922-01) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2018-04-13 |
| 00024-5922-02 | 2 SYRINGE in 1 PACKAGE (0024-5922-02) / 1.14 mL in 1 SYRING... | KEVZARA | Sanofi-Aventis U.S. LLC | 2018-04-13 |
Observed labelers:
Sanofi-Aventis U.S. LLC (8)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ 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.