Selumetinib 25 MG Oral Capsule — RxCUI 2289426
RxNorm drug concept · Semantic clinical drug
RxCUI 2289426
Semantic clinical drug · SCD
● Current RxNorm concept 4 FDA products
6 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
RxCUI2289426
Official nameSelumetinib 25 MG Oral Capsule
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asselumetinib (as selumetinib sulfate) 25 MG Oral Capsule
FDA products mapped4
Package NDCs mapped6
Reported Medicaid activity (SDUD)3,980 prescriptions · 28 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 Selumetinib: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
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- What exactly is this medication treating — and will it cure my (or my child's) NF1 tumors?
- Most people experience some side effects — diarrhea, nausea, vomiting, and skin rashes (sometimes acne-like) are the most common. These are often manageable: for diarrhea, start an...
- What side effects should I realistically expect, and which ones should I call the doctor about right away?
🕸️ Concept Web — How Selumetinib 25 MG Oral Capsule 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
Selumetinib 25 MG Oral Capsule
RxCUI 2289426 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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Selumetinib
2289380IN
-
Selumetinib
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Koselugo
2289419BN
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Koselugo
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Selumetinib Oral Capsule
2289417SCDF -
Selumetinib Oral Product
2289415SCDG -
Selumetinib Pill
2289416SCDG -
Selumetinib Oral Capsule [Koselugo]
2289421SBDF -
Koselugo Oral Product
2289422SBDG -
Koselugo Pill
2289423SBDG -
Oral Capsule
316965DF -
Oral Product
1151131DFG - +1 more in this family
-
Selumetinib Oral Capsule
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Selumetinib 25 MG
2289425SCDC -
Selumetinib 25 MG Oral Capsule [Koselugo]
2289428SBD -
Selumetinib 25 MG [Koselugo]
2289427SBDC
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Selumetinib 25 MG
Showing up to 8 concepts per family — 13 of 14 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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Selumetinib 25 MG
SCDC · 2289425 -
Selumetinib Oral Capsule
SCDF · 2289417 -
Selumetinib Oral Product
SCDG · 2289415 -
Selumetinib Pill
SCDG · 2289416
Brand-Name Concepts
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Selumetinib 25 MG Oral Capsule [Koselugo]
SBD · 2289428 -
Selumetinib 25 MG [Koselugo]
SBDC · 2289427 -
Selumetinib Oral Capsule [Koselugo]
SBDF · 2289421 -
Koselugo Oral Product
SBDG · 2289422 -
Koselugo Pill
SBDG · 2289423 -
Koselugo
BN · 2289419
📦 FDA Products & Package NDCs
4 products · 6 package NDCs
6 package NDCs map to RxCUI 2289426 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 |
|---|---|---|---|---|
| 00310-0610-28 | 28 CAPSULE in 1 BOTTLE (0310-0610-28) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2021-06-11 |
| 00310-0610-60 | 60 CAPSULE in 1 BOTTLE (0310-0610-60) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2020-04-16 |
| 00310-0625-28 | 28 CAPSULE in 1 BOTTLE (0310-0625-28) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2021-06-11 |
| 00310-0625-60 | 60 CAPSULE in 1 BOTTLE (0310-0625-60) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2020-04-16 |
| 00310-0635-60 | 60 GRANULE in 1 BOTTLE (0310-0635-60) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2025-09-10 |
| 00310-0640-60 | 60 GRANULE in 1 BOTTLE (0310-0640-60) | KOSELUGO | AstraZeneca Pharmaceuticals LP | 2025-09-10 |
Observed labelers:
AstraZeneca Pharmaceuticals LP (6)
— 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.