Naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet [Treximet] — RxCUI 849452
RxNorm drug concept · Semantic branded drug
RxCUI 849452
Semantic branded drug · SBD
● 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
RxCUI849452
Official nameNaproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet [Treximet]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asTreximet 85/500 (sumitriptan / naproxen sodium) Oral Tablet; Treximet 85 MG / 500 MG Oral Tablet; Treximet (naproxen sodium 500 MG / sumatriptan 85 MG (as sumatriptan succinate 119 MG)) Oral Tablet
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Sumatriptan: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Sumatriptan is specifically for migraine headaches — it's not a general pain reliever like ibuprofen. It's designed to stop a migraine attack once it's already started, with or wit...
- What exactly is sumatriptan for? Will it work on any headache?
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- When should I take sumatriptan — do I have to wait until the headache is severe?
🕸️ Concept Web — How Naproxen sodium 500 MG / sumatriptan 85 MG Oral... 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
Naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet [Treximet]
RxCUI 849452 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 4
The active substance itself — no strength, form, or brand attached yet.
-
Naproxen
7258IN -
Sumatriptan
37418IN -
Naproxen / sumatriptan
797426MIN -
Naproxen sodium
142442PIN
-
Naproxen
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Treximet
794765BN
-
Treximet
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Naproxen / sumatriptan Oral Tablet
794763SCDF -
Naproxen sodium / sumatriptan Oral Tablet
2647518SCDFP -
Naproxen / sumatriptan Oral Product
1157005SCDG -
Naproxen / sumatriptan Pill
1157512SCDG -
Naproxen sodium / sumatriptan Oral Product
2661109SCDGP -
Naproxen sodium / sumatriptan Pill
2661991SCDGP -
Naproxen / sumatriptan Oral Tablet [Treximet]
794767SBDF -
Naproxen sodium / sumatriptan Oral Tablet [Treximet]
2654512SBDFP - +5 more in this family
-
Naproxen / sumatriptan Oral Tablet
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet
849450SCD -
Naproxen sodium 500 MG
849449SCDC -
Sumatriptan 85 MG
644919SCDC -
Naproxen sodium 500 MG / sumatriptan 85 MG [Treximet]
849451SBDC
-
Naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet
Showing up to 8 concepts per family — 17 of 22 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
-
Naproxen sodium 500 MG / sumatriptan 85 MG Oral Tablet
SCD · 849450 -
Naproxen sodium 500 MG
SCDC · 849449 -
Sumatriptan 85 MG
SCDC · 644919 -
Naproxen / sumatriptan Oral Tablet
SCDF · 794763 -
Naproxen sodium / sumatriptan Oral Tablet
SCDFP · 2647518 -
Naproxen / sumatriptan Oral Product
SCDG · 1157005 -
Naproxen / sumatriptan Pill
SCDG · 1157512 -
Naproxen sodium / sumatriptan Oral Product
SCDGP · 2661109 -
Naproxen sodium / sumatriptan Pill
SCDGP · 2661991
Brand-Name Concepts
-
Naproxen sodium 500 MG / sumatriptan 85 MG [Treximet]
SBDC · 849451 -
Naproxen / sumatriptan Oral Tablet [Treximet]
SBDF · 794767 -
Naproxen sodium / sumatriptan Oral Tablet [Treximet]
SBDFP · 2654512 -
Treximet Oral Product
SBDG · 1179685 -
Treximet Pill
SBDG · 1179686 -
Treximet
BN · 794765
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 849452 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 |
|---|---|---|---|---|
| 42847-0850-09 | 9 TABLET, FILM COATED in 1 BOTTLE (42847-850-09) | Treximet | Currax Pharmaceuticals LLC | 2008-04-25 |
Observed labelers:
Currax Pharmaceuticals LLC (1)
— 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.