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24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension — RxCUI 1312583

RxNorm drug concept · Semantic clinical drug
RxCUI 1312583 Semantic clinical drug · SCD ● Current RxNorm concept 4 FDA products 4 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

RxCUI1312583
Official name24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asmethylphenidate HCl 25 MG in 5 mL 24HR Extended Release Oral Suspension; methylphenidate hydrochloride 25 MG per 5 ML 24 HR Extended Release Suspension
FDA products mapped4
Package NDCs mapped4
Reported Medicaid activity (SDUD)227,841 prescriptions · 47 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

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🕸️ Concept Web — How 24 HR methylphenidate hydrochloride 5 MG/ML Exte... 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 24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension RxCUI 1312583

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

  1. Ingredients 2

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

    • Methylphenidate 6901
    • Methylphenidate hydrochloride 203188
  2. Brand names 1

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

    • Quillivant 1312584
  3. Dose forms 13

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

    • Methylphenidate Extended Release Suspension 1312582
    • Methylphenidate hydrochloride Extended Release Suspension 2647892
    • Methylphenidate Oral Liquid Product 1162890
    • Methylphenidate Oral Product 1163482
    • Methylphenidate hydrochloride Oral Liquid Product 2661150
    • Methylphenidate hydrochloride Oral Product 2661865
    • Methylphenidate Extended Release Suspension [Quillivant] 1312586
    • Methylphenidate hydrochloride Extended Release Suspension [Quillivant] 2657951
    • +5 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 — 14 of 19 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

  • Methylphenidate hydrochloride 5 MG/ML SCDC · 1312581
  • Methylphenidate Extended Release Suspension SCDF · 1312582
  • Methylphenidate hydrochloride Extended Release Suspension SCDFP · 2647892
  • Methylphenidate Oral Liquid Product SCDG · 1162890
  • Methylphenidate Oral Product SCDG · 1163482
  • Methylphenidate hydrochloride Oral Liquid Product SCDGP · 2661150
  • Methylphenidate hydrochloride Oral Product SCDGP · 2661865

Brand-Name Concepts

  • 24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension [Quillivant] SBD · 1312589
  • Methylphenidate hydrochloride 5 MG/ML [Quillivant] SBDC · 1312585
  • Methylphenidate Extended Release Suspension [Quillivant] SBDF · 1312586
  • Methylphenidate hydrochloride Extended Release Suspension [Quillivant] SBDFP · 2657951
  • Quillivant Oral Liquid Product SBDG · 1312587
  • Quillivant Oral Product SBDG · 1312588
  • Quillivant BN · 1312584

📦 FDA Products & Package NDCs

4 products · 4 package NDCs
4 package NDCs map to RxCUI 1312583 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
24478-0321-02 1 BOTTLE in 1 CARTON (24478-321-02) / 60 mL in 1 BOTTLE Quillivant XR NextWave Pharmaceuticals, Inc 2012-10-01
24478-0322-04 1 BOTTLE in 1 CARTON (24478-322-04) / 120 mL in 1 BOTTLE Quillivant XR NextWave Pharmaceuticals, Inc 2012-10-01
24478-0323-05 1 BOTTLE in 1 CARTON (24478-323-05) / 150 mL in 1 BOTTLE Quillivant XR NextWave Pharmaceuticals, Inc 2012-10-01
24478-0324-06 1 BOTTLE in 1 CARTON (24478-324-06) / 180 mL in 1 BOTTLE Quillivant XR NextWave Pharmaceuticals, Inc 2013-01-04
Observed labelers: NextWave Pharmaceuticals, Inc (4) — 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.