Alogliptin

Orange BookUNIISPLATC A10BH04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA10BH04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6362949461
30 TABLET, FILM COATED in 1 BOTTLE (63629-4946-1)

Annotations

UNII (FDA Substance ID)

EEN99869SC

ALOGLIPTIN BENZOATE

RxCUI 1368000

Orange Book

N022271

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "EEN99869SC",
    "rxcui": "1368000",
    "inchikey": "KEJICOXJTRHYAK-XFULWGLBSA-N",
    "display_name": "ALOGLIPTIN BENZOATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "642b1e90-701e-42f2-bac6-a4918738e2c9": {
      "match": "brand_token",
      "title": "ALOGLIPTIN AND PIOGLITAZONE (ALOGLIPTIN BENZOATE AND PIOGLITAZONE HYDROCHLORIDE) TABLET, FILM COATED [PADAGIS ISRAEL PHARMACEUTICALS LTD]",
      "spl_version": "11",
      "published_date": "2025-08-11"
    }
  },
  "productid": "63629-4946_92219b66-aacf-4ddc-9320-9ea8f620ab8c",
  "productndc": "63629-4946",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "022271",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "EQ 6.25MG BASE",
        "product_no": "001",
        "approval_date": "Jan 25, 2013"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "EQ 12.5MG BASE",
        "product_no": "002",
        "approval_date": "Jan 25, 2013"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "EQ 25MG BASE",
        "product_no": "003",
        "approval_date": "Jan 25, 2013"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ALOGLIPTIN BENZOATE",
  "proprietary_name": "Alogliptin",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA022271",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "Alogliptin",
  "start_marketing_date": "20160408",
  "active_numerator_strength": "25"
}

Related drugs

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