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United States · US · US:51662-1217_120072e0-4439-faf9-e063-6294a90a3ad1
DIGOXIN
Orange BookUNIISPLATC C01AA05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHF Acquisition Co LLC, DBA HealthFirst
CountryUS (United States)
ATC codeC01AA05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1151662121712 mL in 1 AMPULE (51662-1217-1)
- ndc11516621217325 POUCH in 1 CASE (51662-1217-3) / 1 mL in 1 POUCH (51662-1217-2)
Annotations
UNII (FDA Substance ID)
73K4184T59
DIGOXIN
RxCUI 3407
Orange Book
A083391
AP
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": "INTRAMUSCULAR; INTRAVENOUS",
"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": "51662-1217_120072e0-4439-faf9-e063-6294a90a3ad1",
"productndc": "51662-1217",
"dosage_form": "INJECTION",
"orange_book": {
"appl_no": "083391",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "0.25MG/ML",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIGOXIN",
"proprietary_name": "DIGOXIN",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA083391",
"marketing_category": "ANDA",
"nonproprietary_name": "DIGOXIN",
"start_marketing_date": "20180913",
"active_numerator_strength": ".25"
}Related drugs
Other records sharing ATC code C01AA05.
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