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United States · US · US:64842-0727_130350a1-2b88-4253-99ea-9fbc0d066ea7
INQOVI
Orange BookUNIISPLATC L01BC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTaiho Pharmaceutical Co., Ltd.
CountryUS (United States)
ATC codeL01BC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1164842072791 BLISTER PACK in 1 CARTON (64842-0727-9) / 5 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
39IS23Q1EW
CEDAZURIDINE
RxCUI 2384449
Orange Book
N212576
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "39IS23Q1EW",
"rxcui": "2384449",
"inchikey": "VUDZSIYXZUYWSC-DBRKOABJSA-N",
"display_name": "CEDAZURIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"91a0f80b-f865-4d06-a40d-4d148d99ee71": {
"match": "brand_token",
"title": "INQOVI (CEDAZURIDINE AND DECITABINE) TABLET, FILM COATED [TAIHO PHARMACEUTICAL CO., LTD.]",
"spl_version": "13",
"published_date": "2026-05-28"
}
},
"productid": "64842-0727_130350a1-2b88-4253-99ea-9fbc0d066ea7",
"productndc": "64842-0727",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "212576",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "100MG;35MG",
"product_no": "001",
"approval_date": "Jul 7, 2020"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEDAZURIDINE; DECITABINE",
"proprietary_name": "INQOVI",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "NDA212576",
"marketing_category": "NDA",
"nonproprietary_name": "CEDAZURIDINE and DECITABINE",
"start_marketing_date": "20200707",
"active_numerator_strength": "100; 35"
}Related drugs
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