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United States · US · US:50228-513_3b53cebf-946d-b82b-e063-6394a90a5da7

Rivaroxaban

Orange BookUNIISPLATC B01AF01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerScieGen pharmaceuticals,Inc
CountryUS (United States)
ATC codeB01AF01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    5022851318
    180 TABLET, FILM COATED in 1 BOTTLE (50228-513-18)
  • ndc11
    5022851360
    60 TABLET, FILM COATED in 1 BOTTLE (50228-513-60)

Annotations

UNII (FDA Substance ID)
9NDF7JZ4M3
RIVAROXABAN
RxCUI 1114195
Orange Book
A218117
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9NDF7JZ4M3",
    "rxcui": "1114195",
    "inchikey": "KGFYHTZWPPHNLQ-AWEZNQCLSA-N",
    "display_name": "RIVAROXABAN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "925a9a11-ae5b-405c-96d2-b1be4b85bf71": {
      "match": "brand_token",
      "title": "RIVAROXABAN TABLET, COATED [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
      "spl_version": "15",
      "published_date": "2026-05-28"
    }
  },
  "productid": "50228-513_3b53cebf-946d-b82b-e063-6394a90a5da7",
  "productndc": "50228-513",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "218117",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Jul 31, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Jul 31, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "003",
        "approval_date": "Jul 31, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "004",
        "approval_date": "Jul 31, 2025"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "RIVAROXABAN",
  "proprietary_name": "Rivaroxaban",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA218117",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Rivaroxaban",
  "start_marketing_date": "20250804",
  "active_numerator_strength": "2.5"
}

Related drugs

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