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Emtricitabine 200 MG / tenofovir alafenamide 25 MG Oral Tablet — RxCUI 1747691

RxNorm drug concept · Semantic clinical drug
RxCUI 1747691 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 3 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

RxCUI1747691
Official nameEmtricitabine 200 MG / tenofovir alafenamide 25 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped2
Package NDCs mapped3
Reported Medicaid activity (SDUD)181,771 prescriptions · 51 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

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Our pharmacist-built guide to Emtricitabine: what it is, how it’s used, side effects, and interactions.

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📖 Read our full Emtricitabine guide →

🕸️ Concept Web — How Emtricitabine 200 MG / tenofovir alafenamide 25... 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 Emtricitabine 200 MG / tenofovir alafenamide 25 MG Oral Tablet RxCUI 1747691

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 3

    The active substance itself — no strength, form, or brand attached yet.

    • Emtricitabine 276237
    • Tenofovir alafenamide 1721603
    • Emtricitabine / tenofovir alafenamide 1727491
  2. Brand names 1

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

    • Descovy 1747692
  3. Dose forms 9

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

    • Emtricitabine / tenofovir alafenamide Oral Tablet 1747690
    • Emtricitabine / tenofovir alafenamide Oral Product 1747688
    • Emtricitabine / tenofovir alafenamide Pill 1747689
    • Emtricitabine / tenofovir alafenamide Oral Tablet [Descovy] 1747694
    • Descovy Oral Product 1747695
    • Descovy Pill 1747696
    • Oral Tablet 317541
    • Oral Product 1151131
    • +1 more in this family
  4. Clinical & branded drugs 4

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

Showing up to 8 concepts per family — 16 of 17 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

  • Emtricitabine 200 MG SCDC · 406016
  • Tenofovir alafenamide 25 MG SCDC · 1741729
  • Emtricitabine / tenofovir alafenamide Oral Tablet SCDF · 1747690
  • Emtricitabine / tenofovir alafenamide Oral Product SCDG · 1747688
  • Emtricitabine / tenofovir alafenamide Pill SCDG · 1747689

Brand-Name Concepts

📦 FDA Products & Package NDCs

2 products · 3 package NDCs
3 package NDCs map to RxCUI 1747691 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
61958-2002-01 30 TABLET in 1 BOTTLE, PLASTIC (61958-2002-1) DESCOVY Gilead Sciences, Inc. 2016-04-04
61958-2002-02 30 TABLET in 1 BLISTER PACK (61958-2002-2) DESCOVY Gilead Sciences, Inc. 2020-01-22
61958-2005-01 30 TABLET in 1 BOTTLE, PLASTIC (61958-2005-1) DESCOVY Gilead Sciences, Inc. 2022-01-07
Observed labelers: Gilead Sciences, Inc. (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.

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.