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Dabigatran etexilate 110 MG Oral Capsule [Pradaxa] — RxCUI 1723478

RxNorm drug concept · Semantic branded drug
RxCUI 1723478 Semantic branded drug · SBD ● Current RxNorm concept 3 FDA products 6 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

RxCUI1723478
Official nameDabigatran etexilate 110 MG Oral Capsule [Pradaxa]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asPradaxa 110 MG Oral Capsule; Pradaxa 110 MG (as dabigatran etexilate mesylate 126.83 MG) Oral Capsule
FDA products mapped3
Package NDCs mapped6
Reported Medicaid activity (SDUD)16,275 prescriptions · 34 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 Dabigatran Etexilate: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It's a blood thinner — its main jobs are to reduce your risk of stroke if you have atrial fibrillation (an irregular heartbeat), to treat or prevent dangerous blood clots in your v...
  • What exactly is dabigatran etexilate used for?
  • No — please don't. Opening, breaking, or chewing the capsule releases the pellets inside in a way the body absorbs about 75% more drug than it should. That raises your risk of seri...
  • Can I open or crush the capsule if I have trouble swallowing it?
📖 Read our full Dabigatran Etexilate guide →

🕸️ Concept Web — How Dabigatran etexilate 110 MG Oral Capsule [Pradax... 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 Dabigatran etexilate 110 MG Oral Capsule [Pradaxa] RxCUI 1723478

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.

    • Dabigatran etexilate 1037042
  2. Brand names 1

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

    • Pradaxa 1037046
  3. Dose forms 9

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

    • Dabigatran etexilate Oral Capsule 1037044
    • Dabigatran etexilate Oral Product 1156646
    • Dabigatran etexilate Pill 1156647
    • Dabigatran etexilate Oral Capsule [Pradaxa] 1037048
    • Pradaxa Oral Product 1184616
    • Pradaxa Pill 1184617
    • Oral Capsule 316965
    • Oral Product 1151131
    • +1 more in this family
  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 — 13 of 14 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

  • Dabigatran etexilate 110 MG Oral Capsule SCD · 1723476
  • Dabigatran etexilate 110 MG SCDC · 1723475
  • Dabigatran etexilate Oral Capsule SCDF · 1037044
  • Dabigatran etexilate Oral Product SCDG · 1156646
  • Dabigatran etexilate Pill SCDG · 1156647

Brand-Name Concepts

  • Dabigatran etexilate 110 MG [Pradaxa] SBDC · 1723477
  • Dabigatran etexilate Oral Capsule [Pradaxa] SBDF · 1037048
  • Pradaxa Oral Product SBDG · 1184616
  • Pradaxa Pill SBDG · 1184617
  • Pradaxa BN · 1037046

📦 FDA Products & Package NDCs

3 products · 6 package NDCs
6 package NDCs map to RxCUI 1723478 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
00597-0108-54 1 BOTTLE in 1 CARTON (0597-0108-54) / 60 CAPSULE in 1 BOTTL... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2017-07-07
00597-0108-60 10 BLISTER PACK in 1 CARTON (0597-0108-60) / 6 CAPSULE in 1... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2015-11-23
00597-0355-09 1 BOTTLE in 1 CARTON (0597-0355-09) / 60 CAPSULE in 1 BOTTL... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2017-07-28
00597-0355-56 60 BLISTER PACK in 1 CARTON (0597-0355-56) / 1 CAPSULE in 1... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2017-07-28
00597-0360-55 1 BOTTLE in 1 CARTON (0597-0360-55) / 60 CAPSULE in 1 BOTTL... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2017-07-28
00597-0360-82 60 BLISTER PACK in 1 CARTON (0597-0360-82) / 1 CAPSULE in 1... Pradaxa Boehringer Ingelheim Pharmaceuticals Inc. 2017-07-28
Observed labelers: Boehringer Ingelheim Pharmaceuticals Inc. (6) — 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.

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.