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United States · US · US:59651-436_1338ce78-5a23-4dd2-bb1b-335f35cb2646
Digoxin
Orange BookUNIISPLATC C01AA05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC codeC01AA05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc115965143601100 TABLET in 1 BOTTLE (59651-436-01)
- ndc1159651436991000 TABLET in 1 BOTTLE (59651-436-99)
Annotations
UNII (FDA Substance ID)
73K4184T59
DIGOXIN
RxCUI 3407
Orange Book
A214982
ABABAB
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": "59651-436_1338ce78-5a23-4dd2-bb1b-335f35cb2646",
"productndc": "59651-436",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "214982",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.0625MG",
"product_no": "001",
"approval_date": "Feb 8, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.125MG",
"product_no": "002",
"approval_date": "Feb 8, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "003",
"approval_date": "Feb 8, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIGOXIN",
"proprietary_name": "Digoxin",
"active_ingred_unit": "mg/1",
"application_number": "ANDA214982",
"marketing_category": "ANDA",
"nonproprietary_name": "Digoxin",
"start_marketing_date": "20220208",
"active_numerator_strength": ".0625"
}Related drugs
Other records sharing ATC code C01AA05.
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