60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler — RxCUI 896025
RxNorm drug concept · Semantic clinical drug
RxCUI 896025
Semantic clinical drug · SCD
● Current RxNorm concept 3 FDA products
3 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
RxCUI896025
Official name60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asfluticasone propionate 250 MCG/INHAL Dry Powder Inhaler, 60 Blisters
FDA products mapped3
Package NDCs mapped3
Reported Medicaid activity (SDUD)29,142 prescriptions · 37 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 Fluticasone Oral Inhalation: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- No — fluticasone is a preventive inhaler, not a rescue inhaler. It works by slowly reducing airway inflammation over days to weeks, so it won't open your airways fast enough during...
- Can I use my fluticasone inhaler when I'm having an asthma attack?
- Great question — this is one of the most practical things you can do. When you inhale fluticasone, some of the medication can land in your mouth and throat rather than making it al...
- Why do I need to rinse my mouth after using it?
🕸️ Concept Web — How 60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT... 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
60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler
RxCUI 896025 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
-
Fluticasone
41126IN -
Fluticasone propionate
50121PIN
-
Fluticasone
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Flovent
217152BN
-
Flovent
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Fluticasone Dry Powder Inhaler
746765SCDF -
Fluticasone propionate Dry Powder Inhaler
2648024SCDFP -
Fluticasone Inhalant Product
1165655SCDG -
Fluticasone propionate Inhalant Product
2662132SCDGP -
Fluticasone Dry Powder Inhaler [Flovent]
746805SBDF -
Fluticasone propionate Dry Powder Inhaler [Flovent]
2657336SBDFP -
Flovent Inhalant Product
1169793SBDG -
Dry Powder Inhaler
744995DF - +1 more in this family
-
Fluticasone Dry Powder Inhaler
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Fluticasone propionate 0.25 MG/ACTUAT
896024SCDC -
60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler [Flovent]
896027SBD -
Fluticasone propionate 0.25 MG/ACTUAT [Flovent]
896026SBDC
-
Fluticasone propionate 0.25 MG/ACTUAT
Showing up to 8 concepts per family — 14 of 15 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
-
Fluticasone propionate 0.25 MG/ACTUAT
SCDC · 896024 -
Fluticasone Dry Powder Inhaler
SCDF · 746765 -
Fluticasone propionate Dry Powder Inhaler
SCDFP · 2648024 -
Fluticasone Inhalant Product
SCDG · 1165655 -
Fluticasone propionate Inhalant Product
SCDGP · 2662132
Brand-Name Concepts
-
60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler [Flovent]
SBD · 896027 -
Fluticasone propionate 0.25 MG/ACTUAT [Flovent]
SBDC · 896026 -
Fluticasone Dry Powder Inhaler [Flovent]
SBDF · 746805 -
Fluticasone propionate Dry Powder Inhaler [Flovent]
SBDFP · 2657336 -
Flovent Inhalant Product
SBDG · 1169793 -
Flovent
BN · 217152
📦 FDA Products & Package NDCs
3 products · 3 package NDCs
3 package NDCs map to RxCUI 896025 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 |
|---|---|---|---|---|
| 66993-0790-97 | 1 INHALER in 1 CARTON (66993-790-97) / 60 POWDER, METERED i... | FLUTICASONE PROPIONATE DISKUS | Prasco Laboratories | 2023-10-30 |
| 66993-0791-97 | 1 INHALER in 1 CARTON (66993-791-97) / 60 POWDER, METERED i... | FLUTICASONE PROPIONATE DISKUS | Prasco Laboratories | 2023-10-30 |
| 66993-0792-97 | 1 INHALER in 1 CARTON (66993-792-97) / 60 POWDER, METERED i... | FLUTICASONE PROPIONATE DISKUS | Prasco Laboratories | 2023-10-30 |
Observed labelers:
Prasco Laboratories (3)
— 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.