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Ubrogepant 100 MG Oral Tablet — RxCUI 2268221

RxNorm drug concept · Semantic clinical drug
RxCUI 2268221 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 9 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

RxCUI2268221
Official nameUbrogepant 100 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped2
Package NDCs mapped9
Reported Medicaid activity (SDUD)329,850 prescriptions · 52 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 Ubrogepant: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It treats a migraine attack in adults once it has started, with or without aura. It is not meant to prevent migraines, so it won't reduce how often you get them.
  • Swallow the tablet when a migraine starts. You can take it with or without food. If you need it, a second dose can be taken at least 2 hours after the first. Follow the dose your p...
  • The most common are nausea, sleepiness and dry mouth. Because of the sleepiness, notice how it affects you before doing anything that needs full alertness.
  • Get help right away for trouble breathing, or swelling of your face or throat, hives or rash, and stop the medicine. Also call if you notice high blood pressure or fingers or toes...
📖 Read our full Ubrogepant guide →

🕸️ Concept Web — How Ubrogepant 100 MG Oral Tablet 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 Ubrogepant 100 MG Oral Tablet RxCUI 2268221

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

  1. Ingredients 1

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

    • Ubrogepant 2268216
  2. Brand names 1

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

    • Ubrelvy 2268222
  3. Dose forms 9

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

    • Ubrogepant Oral Tablet 2268220
    • Ubrogepant Oral Product 2268218
    • Ubrogepant Pill 2268219
    • Ubrogepant Oral Tablet [Ubrelvy] 2268224
    • Ubrelvy Oral Product 2268225
    • Ubrelvy Pill 2268226
    • Oral Tablet 317541
    • Oral Product 1151131
    • +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 — 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

  • Ubrogepant 100 MG SCDC · 2268217
  • Ubrogepant Oral Tablet SCDF · 2268220
  • Ubrogepant Oral Product SCDG · 2268218
  • Ubrogepant Pill SCDG · 2268219

Brand-Name Concepts

  • Ubrogepant 100 MG Oral Tablet [Ubrelvy] SBD · 2268227
  • Ubrogepant 100 MG [Ubrelvy] SBDC · 2268223
  • Ubrogepant Oral Tablet [Ubrelvy] SBDF · 2268224
  • Ubrelvy Oral Product SBDG · 2268225
  • Ubrelvy Pill SBDG · 2268226
  • Ubrelvy BN · 2268222

📦 FDA Products & Package NDCs

2 products · 9 package NDCs
9 package NDCs map to RxCUI 2268221 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
00023-6498-01 1 PACKET in 1 BOX (0023-6498-01) / 1 TABLET in 1 PACKET UBRELVY Allergan, Inc. 2019-12-23
00023-6498-04 4 PACKET in 1 BOX (0023-6498-04) / 1 TABLET in 1 PACKET UBRELVY Allergan, Inc. 2019-12-23
00023-6498-10 10 PACKET in 1 BOX (0023-6498-10) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
00023-6498-16 16 PACKET in 1 BOX (0023-6498-16) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
00023-6498-30 30 PACKET in 1 BOX (0023-6498-30) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
00023-6501-01 1 PACKET in 1 BOX (0023-6501-01) / 1 TABLET in 1 PACKET UBRELVY Allergan, Inc. 2019-12-23
00023-6501-10 10 PACKET in 1 BOX (0023-6501-10) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
00023-6501-16 16 PACKET in 1 BOX (0023-6501-16) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
00023-6501-30 30 PACKET in 1 BOX (0023-6501-30) / 1 TABLET in 1 PACKET (0... UBRELVY Allergan, Inc. 2019-12-23
Observed labelers: Allergan, Inc. (9) — 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.

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.