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United States · US · US:46708-346_4b61dc52-0593-4ef0-8246-a82ff6972842
RIVAROXABAN
Orange BookUNIISPLATC B01AF01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Limited
CountryUS (United States)
ATC codeB01AF01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc114670834610100 BLISTER PACK in 1 CARTON (46708-346-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- ndc11467083463030 TABLET, FILM COATED in 1 BOTTLE (46708-346-30)
- ndc11467083469090 TABLET, FILM COATED in 1 BOTTLE (46708-346-90)
- ndc1146708346911000 TABLET, FILM COATED in 1 BOTTLE (46708-346-91)
Annotations
UNII (FDA Substance ID)
9NDF7JZ4M3
RIVAROXABAN
RxCUI 1114195
Orange Book
A210301
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": "46708-346_4b61dc52-0593-4ef0-8246-a82ff6972842",
"productndc": "46708-346",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "210301",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "May 14, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "002",
"approval_date": "May 14, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "003",
"approval_date": "May 14, 2025"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "004",
"approval_date": "May 14, 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": "ANDA210301",
"marketing_category": "ANDA",
"nonproprietary_name": "RIVAROXABAN",
"start_marketing_date": "20250514",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code B01AF01.
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