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United States · US · US:72162-2268_d3d58857-c095-44ef-8ff6-f4a2a5d781e1
Digoxin
Orange BookUNIISPLATC C01AA05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC01AA05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1172162226801000 TABLET in 1 BOTTLE (72162-2268-0)
- ndc117216222681100 TABLET in 1 BOTTLE (72162-2268-1)
- ndc1172162226821000 TABLET in 1 BOTTLE (72162-2268-2)
- ndc117216222684100 TABLET in 1 BOTTLE (72162-2268-4)
Annotations
UNII (FDA Substance ID)
73K4184T59
DIGOXIN
RxCUI 3407
Orange Book
A076268
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "73K4184T59",
"rxcui": "3407",
"inchikey": "LTMHDMANZUZIPE-PUGKRICDSA-N",
"display_name": "DIGOXIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"5fb1bc4e-5806-4c50-aab0-91e445d87933": {
"match": "brand_token",
"title": "DIGOXIN TABLET [BRYANT RANCH PREPACK]",
"spl_version": "103",
"published_date": "2026-05-11"
}
},
"productid": "72162-2268_d3d58857-c095-44ef-8ff6-f4a2a5d781e1",
"productndc": "72162-2268",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "076268",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.125MG",
"product_no": "001",
"approval_date": "Jul 26, 2002"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "002",
"approval_date": "Jul 26, 2002"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIGOXIN",
"proprietary_name": "Digoxin",
"active_ingred_unit": "ug/1",
"application_number": "ANDA076268",
"marketing_category": "ANDA",
"nonproprietary_name": "Digoxin",
"start_marketing_date": "20220901",
"active_numerator_strength": "125"
}Related drugs
Other records sharing ATC code C01AA05.
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