Home › NDC Lookup › RxCUI directory › RxCUI 1649961

200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir] — RxCUI 1649961

RxNorm drug concept · Semantic branded drug
RxCUI 1649961 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 1 package NDC Snapshot Jul 14, 2026

This page is curated, coded, and maintained by

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

RxCUI1649961
Official name200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known as200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler; ProAir RespiClick 90 MCG/INHAL Dry Powder Inhaler, 200 Actuations; ProAir RespiClick 90 MCG/ACTUAT (albuterol sulfate 108 MCG/ACTUAT from mouthpiece) Dry Powder Inhaler, 200 ACTUAT; ProAir RespiClick 90 MCG/ACTUAT Dry Powder Inhaler, 200 ACTUAT
FDA products mapped1
Package NDCs mapped1
Reported Medicaid activity (SDUD)64,756 prescriptions · 46 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 Albuterol: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Albuterol opens up your airways when the muscles around them tighten (bronchospasm), as in asthma. Inhalers and powders are also used before exercise to prevent exercise-induced br...
  • It is breathed in through your mouth. The usual pattern for bronchospasm is a couple of puffs every 4 to 6 hours, and before exercise it is used 15 to 30 minutes ahead. Some inhale...
  • The most common are throat irritation, cough, upper respiratory irritation, viral respiratory infections and muscle or bone aches. These are usually manageable. Call me or your doc...
  • Get help right away if your breathing gets worse after a dose, or if you have hives, swelling of the face or throat, or chest pain or a racing heartbeat. Also call your doctor if y...
📖 Read our full Albuterol guide →

🕸️ Concept Web — How 200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder I... 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 200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir] RxCUI 1649961

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.

    • Albuterol 435
  2. Brand names 1

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

    • ProAir 647295
  3. Dose forms 6

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

    • Albuterol Dry Powder Inhaler 1649559
    • Albuterol Inhalant Product 1154602
    • Albuterol Dry Powder Inhaler [ProAir] 1649959
    • ProAir Inhalant Product 1649960
    • Dry Powder Inhaler 744995
    • Inhalant Product 1151123
  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

Brand-Name Concepts

  • Albuterol 0.09 MG/ACTUAT [ProAir] SBDC · 1649958
  • Albuterol Dry Powder Inhaler [ProAir] SBDF · 1649959
  • ProAir Inhalant Product SBDG · 1649960
  • ProAir BN · 647295

📦 FDA Products & Package NDCs

1 product · 1 package NDC
1 package NDC map to RxCUI 1649961 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
59310-0580-20 1 INHALER in 1 BOX (59310-580-20) / 200 POWDER, METERED in... ProAir RespiClick Teva Respiratory, LLC 2015-05-11
Observed labelers: Teva Respiratory, LLC (1) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

💲 Pricing (NADAC)

NADAC is CMS's National Average Drug Acquisition Cost — roughly what pharmacies pay to buy the drug. It is an acquisition benchmark, not your copay.
Per ea · median
$67.2116
Range $67.2116–$67.2116 · middle 50% $67.2116–$67.2116 · 1 NDCs
Latest compatible distributions from the CMS NADAC file · dataset watermark 2026-07-10. Prices vary by package and pharmacy; a distribution is shown instead of one misleading number. Rows the dataset is silent on carry no price. No zero-cost conclusion should be drawn.

🗃️ 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.