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United States · US · US:50090-5642_0f092467-7f66-1cb2-e063-6394a90a88a2
Digoxin
Orange BookUNIISPLATC C01AA05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeC01AA05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc115009056421100 TABLET in 1 BOTTLE (50090-5642-1)
Annotations
UNII (FDA Substance ID)
73K4184T59
DIGOXIN
RxCUI 3407
Orange Book
A076363
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": "50090-5642_0f092467-7f66-1cb2-e063-6394a90a88a2",
"productndc": "50090-5642",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "076363",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.125MG",
"product_no": "001",
"approval_date": "Jan 31, 2003"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.25MG",
"product_no": "002",
"approval_date": "Jan 31, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIGOXIN",
"proprietary_name": "Digoxin",
"active_ingred_unit": "ug/1",
"application_number": "ANDA076363",
"marketing_category": "ANDA",
"nonproprietary_name": "Digoxin",
"start_marketing_date": "20150217",
"active_numerator_strength": "125"
}Related drugs
Other records sharing ATC code C01AA05.
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