200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler — RxCUI 1649560
RxNorm drug concept · Semantic clinical drug
RxCUI 1649560
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
RxCUI1649560
Official name200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asalbuterol 90 MCG/ACTUAT Dry Powder Inhaler, 200 ACTUAT; albuterol sulfate 90 MCG/INHAL Dry Powder Inhaler, 200 Actuations; albuterol 90 MCG/ACTUAT (albuterol sulfate 108 MCG/ACTUAT from mouthpiece) 200 ACTUAT Dry Powder Inhaler
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...
🕸️ 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
RxCUI 1649560 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Albuterol
435IN
-
Albuterol
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
ProAir
647295BN
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ProAir
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Albuterol Dry Powder Inhaler
1649559SCDF -
Albuterol Inhalant Product
1154602SCDG -
Albuterol Dry Powder Inhaler [ProAir]
1649959SBDF -
ProAir Inhalant Product
1649960SBDG -
Dry Powder Inhaler
744995DF -
Inhalant Product
1151123DFG
-
Albuterol Dry Powder Inhaler
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Albuterol 0.09 MG/ACTUAT
329498SCDC -
200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir]
1649961SBD -
Albuterol 0.09 MG/ACTUAT [ProAir]
1649958SBDC
-
Albuterol 0.09 MG/ACTUAT
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
-
Albuterol 0.09 MG/ACTUAT
SCDC · 329498 -
Albuterol Dry Powder Inhaler
SCDF · 1649559 -
Albuterol Inhalant Product
SCDG · 1154602
Brand-Name Concepts
-
200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir]
SBD · 1649961 -
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 1649560 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.