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United States · US · US:0003-3764_f96cb5ea-74e9-4751-883d-d18ef0d83640
ELIQUIS
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerE.R. Squibb & Sons, L.L.C.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100033764741 KIT in 1 CARTON (0003-3764-74) * 32 TABLET, COATED in 1 BLISTER PACK * 42 TABLET, COATED in 1 BLISTER PACK
Annotations
Orange Book
N202155
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"a454cd24-0c6d-46e8-b1e4-197388606175": {
"match": "brand_token",
"title": "ELIQUIS (APIXABAN) TABLET, FILM COATED [CARDINAL HEALTH 107, LLC]",
"spl_version": "38",
"published_date": "2026-05-04"
}
},
"productid": "0003-3764_f96cb5ea-74e9-4751-883d-d18ef0d83640",
"productndc": "0003-3764",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "202155",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Dec 28, 2012"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "5MG",
"product_no": "002",
"approval_date": "Dec 28, 2012"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "0.5MG",
"product_no": "003",
"approval_date": "Apr 17, 2025"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "ELIQUIS",
"active_ingred_unit": null,
"application_number": "NDA202155",
"marketing_category": "NDA",
"nonproprietary_name": "apixaban",
"start_marketing_date": "20171129",
"active_numerator_strength": null
}Access this data programmatically
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