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Alogliptin 25 MG Oral Tablet [Nesina] — RxCUI 1368012

RxNorm drug concept · Semantic branded drug
RxCUI 1368012 Semantic branded drug · SBD ● Current RxNorm concept 3 FDA products 10 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

RxCUI1368012
Official nameAlogliptin 25 MG Oral Tablet [Nesina]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asNesina 25 MG Oral Tablet; Nesina 25 MG (as alogliptin benzoate 34 MG) Oral Tablet
FDA products mapped3
Package NDCs mapped10
Reported Medicaid activity (SDUD)205 prescriptions · 3 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 Alogliptin: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • After you eat, your gut releases natural hormones that signal your pancreas to release insulin. An enzyme in your body called DPP-4 normally destroys those hormones within minutes....
  • What exactly does alogliptin do — how does it lower my blood sugar?
  • It depends on how well your kidneys are working. Since alogliptin is mostly cleared through the kidneys, your prescriber will likely lower your dose if your kidney function is redu...
  • Can I take alogliptin if I have kidney problems?
📖 Read our full Alogliptin guide →

🕸️ Concept Web — How Alogliptin 25 MG Oral Tablet [Nesina] 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 Alogliptin 25 MG Oral Tablet [Nesina] RxCUI 1368012

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.

    • Alogliptin 1368001
  2. Brand names 1

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

    • Nesina 1368007
  3. Dose forms 9

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

    • Alogliptin Oral Tablet 1368005
    • Alogliptin Oral Product 1368003
    • Alogliptin Pill 1368004
    • Alogliptin Oral Tablet [Nesina] 1368009
    • Nesina Oral Product 1368010
    • Nesina Pill 1368011
    • Oral Tablet 317541
    • 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

  • Alogliptin 25 MG Oral Tablet SCD · 1368006
  • Alogliptin 25 MG SCDC · 1368002
  • Alogliptin Oral Tablet SCDF · 1368005
  • Alogliptin Oral Product SCDG · 1368003
  • Alogliptin Pill SCDG · 1368004

Brand-Name Concepts

  • Alogliptin 25 MG [Nesina] SBDC · 1368008
  • Alogliptin Oral Tablet [Nesina] SBDF · 1368009
  • Nesina Oral Product SBDG · 1368010
  • Nesina Pill SBDG · 1368011
  • Nesina BN · 1368007

📦 FDA Products & Package NDCs

3 products · 10 package NDCs
10 package NDCs map to RxCUI 1368012 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
64764-0125-02 4 CARTON in 1 TRAY (64764-125-02) / 1 BLISTER PACK in 1 CAR... Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0125-30 30 TABLET, FILM COATED in 1 BOTTLE (64764-125-30) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0125-50 500 TABLET, FILM COATED in 1 BOTTLE (64764-125-50) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0125-90 90 TABLET, FILM COATED in 1 BOTTLE (64764-125-90) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0250-02 4 CARTON in 1 TRAY (64764-250-02) / 1 BLISTER PACK in 1 CAR... Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0250-30 30 TABLET, FILM COATED in 1 BOTTLE (64764-250-30) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0250-50 500 TABLET, FILM COATED in 1 BOTTLE (64764-250-50) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0250-90 90 TABLET, FILM COATED in 1 BOTTLE (64764-250-90) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0625-30 30 TABLET, FILM COATED in 1 BOTTLE (64764-625-30) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
64764-0625-90 90 TABLET, FILM COATED in 1 BOTTLE (64764-625-90) Nesina Takeda Pharmaceuticals America, Inc. 2013-01-25
Observed labelers: Takeda Pharmaceuticals America, Inc. (10) — 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.