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Augmented betamethasone 0.0005 MG/MG Topical Gel — RxCUI 848208

RxNorm drug concept · Semantic clinical drug
RxCUI 848208 Semantic clinical drug · SCD ● Current RxNorm concept 1 FDA product 2 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

RxCUI848208
Official nameAugmented betamethasone 0.0005 MG/MG Topical Gel
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asaugmented betamethasone 0.05 % Topical Gel; betamethasone dipropionate 0.05 % Augmented Topical Gel; betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Gel
FDA products mapped1
Package NDCs mapped2
Reported Medicaid activity (SDUD)165 prescriptions · 2 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 Betamethasone Topical: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Betamethasone topical is used for skin conditions that respond to steroid treatment — things like psoriasis, eczema, and other inflammatory skin problems that cause redness and itc...
  • What skin conditions does betamethasone topical treat?
  • Apply a small amount — a thin layer or just a few drops — directly to the affected area once or twice daily, depending on which product you have. Rub it in gently until it disappea...
  • These products are meant for short-term use. In general, you should see improvement within two weeks — if you don't, check back with your doctor rather than continuing on your own....
📖 Read our full Betamethasone Topical guide →

🕸️ Concept Web — How Augmented betamethasone 0.0005 MG/MG Topical Gel 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 Augmented betamethasone 0.0005 MG/MG Topical Gel RxCUI 848208

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.

    • Betamethasone 1514
  2. Dose forms 4

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

    • Betamethasone Topical Gel 377967
    • Betamethasone Topical Product 1153804
    • Topical Gel 346286
    • Topical Product 1151122
  3. Clinical & branded drugs 1

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

    • Betamethasone 0.0005 MG/MG 330632

Showing up to 8 concepts per family — 6 of 6 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

  • Betamethasone 0.0005 MG/MG SCDC · 330632
  • Betamethasone Topical Gel SCDF · 377967
  • Betamethasone Topical Product SCDG · 1153804

📦 FDA Products & Package NDCs

1 product · 2 package NDCs
2 package NDCs map to RxCUI 848208 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
51672-1309-01 1 TUBE in 1 CARTON (51672-1309-1) / 15 g in 1 TUBE Betamethasone Dipropionate Sun Pharmaceutical Industries, Inc. 2003-12-02
51672-1309-03 1 TUBE in 1 CARTON (51672-1309-3) / 50 g in 1 TUBE Betamethasone Dipropionate Sun Pharmaceutical Industries, Inc. 2003-12-02
Observed labelers: Sun Pharmaceutical Industries, Inc. (2) — 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 gm · median
$2.2678
Range $2.0914–$2.4443 · middle 50% $2.1796–$2.3561 · 2 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.