Omaveloxolone 50 MG Oral Capsule — RxCUI 2631936
RxNorm drug concept · Semantic clinical drug
RxCUI 2631936
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
1 package NDC
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
RxCUI2631936
Official nameOmaveloxolone 50 MG Oral Capsule
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped1
Package NDCs mapped1
Reported Medicaid activity (SDUD)515 prescriptions · 19 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
🕸️ Concept Web — How Omaveloxolone 50 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
Omaveloxolone 50 MG Oral Capsule
RxCUI 2631936 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
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Omaveloxolone
2631931IN
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Omaveloxolone
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Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Skyclarys
2631937BN
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Skyclarys
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Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Omaveloxolone Oral Capsule
2631935SCDF -
Omaveloxolone Oral Product
2631933SCDG -
Omaveloxolone Pill
2631934SCDG -
Omaveloxolone Oral Capsule [Skyclarys]
2631941SBDF -
Skyclarys Oral Product
2631939SBDG -
Skyclarys Pill
2631940SBDG -
Oral Capsule
316965DF -
Oral Product
1151131DFG - +1 more in this family
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Omaveloxolone Oral Capsule
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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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Omaveloxolone 50 MG
2631932SCDC -
Omaveloxolone 50 MG Oral Capsule [Skyclarys]
2631942SBD -
Omaveloxolone 50 MG [Skyclarys]
2631938SBDC
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Omaveloxolone 50 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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Omaveloxolone 50 MG
SCDC · 2631932 -
Omaveloxolone Oral Capsule
SCDF · 2631935 -
Omaveloxolone Oral Product
SCDG · 2631933 -
Omaveloxolone Pill
SCDG · 2631934
Brand-Name Concepts
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Omaveloxolone 50 MG Oral Capsule [Skyclarys]
SBD · 2631942 -
Omaveloxolone 50 MG [Skyclarys]
SBDC · 2631938 -
Omaveloxolone Oral Capsule [Skyclarys]
SBDF · 2631941 -
Skyclarys Oral Product
SBDG · 2631939 -
Skyclarys Pill
SBDG · 2631940 -
Skyclarys
BN · 2631937
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 2631936 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 |
|---|---|---|---|---|
| 64406-0250-90 | 90 CAPSULE in 1 BOTTLE (64406-250-90) | SKYCLARYS | Biogen | 2024-11-15 |
Observed labelers:
Biogen (1)
— 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.