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Remifentanil 2 MG Injection [Ultiva] — RxCUI 1729586

RxNorm drug concept · Semantic branded drug
RxCUI 1729586 Semantic branded drug · SBD ● Current RxNorm concept 6 FDA products 6 package NDCs Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

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

RxCUI1729586
Official nameRemifentanil 2 MG Injection [Ultiva]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asUltiva 2 MG Injection
FDA products mapped6
Package NDCs mapped6
Reported Medicaid activity (SDUD)479 prescriptions · 3 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 Remifentanil: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Remifentanil is a specialized opioid used only in surgery and closely monitored settings. It works within seconds and wears off within minutes, which gives your anesthesia team pre...
  • Why am I getting remifentanil instead of a regular pain medicine?
  • Remifentanil controls pain but cannot put you to sleep on its own, so it is always used together with other anesthetics that do cause unconsciousness. Your team combines it with me...
  • Will I be awake or remember anything during surgery if I'm given this?
📖 Read our full Remifentanil guide →

🕸️ Concept Web — How Remifentanil 2 MG Injection [Ultiva] 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 Remifentanil 2 MG Injection [Ultiva] RxCUI 1729586

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.

    • Remifentanil 73032
  2. Brand names 1

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

    • Ultiva 153379
  3. Dose forms 6

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

    • Remifentanil Injection 1729577
    • Remifentanil Injectable Product 1157406
    • Remifentanil Injection [Ultiva] 1729580
    • Ultiva Injectable Product 1187691
    • Injection 1649574
    • Injectable Product 1151126
  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 — 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

  • Remifentanil 2 MG Injection SCD · 1729584
  • Remifentanil 2 MG SCDC · 1729583
  • Remifentanil Injection SCDF · 1729577
  • Remifentanil Injectable Product SCDG · 1157406

Brand-Name Concepts

  • Remifentanil 2 MG [Ultiva] SBDC · 1729585
  • Remifentanil Injection [Ultiva] SBDF · 1729580
  • Ultiva Injectable Product SBDG · 1187691
  • Ultiva BN · 153379

📦 FDA Products & Package NDCs

6 products · 6 package NDCs
6 package NDCs map to RxCUI 1729586 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
67457-0912-01 10 VIAL, GLASS in 1 CARTON (67457-912-01) / 3 mL in 1 VIAL,... Ultiva Mylan Institutional LLC 2020-04-15
67457-0913-02 10 VIAL, GLASS in 1 CARTON (67457-913-02) / 5 mL in 1 VIAL,... Ultiva Mylan Institutional LLC 2020-04-15
67457-0914-05 10 VIAL, GLASS in 1 CARTON (67457-914-05) / 10 mL in 1 VIAL... Ultiva Mylan Institutional LLC 2020-04-15
72078-0034-01 10 VIAL, GLASS in 1 CARTON (72078-034-01) / 3 mL in 1 VIAL,... Ultiva Mylan Institutional LLC 2023-06-21
72078-0035-02 10 VIAL, GLASS in 1 CARTON (72078-035-02) / 5 mL in 1 VIAL,... Ultiva Mylan Institutional LLC 2023-09-18
72078-0036-05 10 VIAL, GLASS in 1 CARTON (72078-036-05) / 10 mL in 1 VIAL... Ultiva Mylan Institutional LLC 2024-12-16
Observed labelers: Mylan Institutional LLC (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.

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.