Gepotidacin 750 MG Oral Tablet — RxCUI 2709218
RxNorm drug concept · Semantic clinical drug
RxCUI 2709218
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
2 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
RxCUI2709218
Official nameGepotidacin 750 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asgepotidacin 750 MG (equivalent to gepotidacin mesylate dihydrate 970.96 MG) Oral Tablet
FDA products mapped1
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
🕸️ Concept Web — How Gepotidacin 750 MG Oral Tablet 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
Gepotidacin 750 MG Oral Tablet
RxCUI 2709218 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
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Gepotidacin
2709212IN
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Gepotidacin
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Blujepa
2709219BN
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Blujepa
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Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Gepotidacin Oral Tablet
2709217SCDF -
Gepotidacin Oral Product
2709215SCDG -
Gepotidacin Pill
2709216SCDG -
Gepotidacin Oral Tablet [Blujepa]
2709223SBDF -
Blujepa Oral Product
2709221SBDG -
Blujepa Pill
2709222SBDG -
Oral Tablet
317541DF -
Oral Product
1151131DFG - +1 more in this family
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Gepotidacin Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Gepotidacin 750 MG
2709214SCDC -
Gepotidacin 750 MG Oral Tablet [Blujepa]
2709224SBD -
Gepotidacin 750 MG [Blujepa]
2709220SBDC
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Gepotidacin 750 MG
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
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Gepotidacin 750 MG
SCDC · 2709214 -
Gepotidacin Oral Tablet
SCDF · 2709217 -
Gepotidacin Oral Product
SCDG · 2709215 -
Gepotidacin Pill
SCDG · 2709216
Brand-Name Concepts
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Gepotidacin 750 MG Oral Tablet [Blujepa]
SBD · 2709224 -
Gepotidacin 750 MG [Blujepa]
SBDC · 2709220 -
Gepotidacin Oral Tablet [Blujepa]
SBDF · 2709223 -
Blujepa Oral Product
SBDG · 2709221 -
Blujepa Pill
SBDG · 2709222 -
Blujepa
BN · 2709219
📦 FDA Products & Package NDCs
1 product · 2 package NDCs
2 package NDCs map to RxCUI 2709218 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 |
|---|---|---|---|---|
| 00173-0922-38 | 8 TABLET, FILM COATED in 1 BOTTLE (0173-0922-38) | Blujepa | GlaxoSmithKline LLC | 2025-12-11 |
| 00173-0922-45 | 20 TABLET, FILM COATED in 1 BOTTLE (0173-0922-45) | Blujepa | GlaxoSmithKline LLC | 2025-03-25 |
Observed labelers:
GlaxoSmithKline LLC (2)
— 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.