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United States · US · US:15631-2718_19ba75a8-51ad-c9f5-e063-6394a90a5214
DIGITALIS PUR
UNIISPLATC C01AA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc
CountryUS (United States)
ATC codeC01AA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11156312718010 mL in 1 BOTTLE (15631-2718-0)
- ndc11156312718130 mL in 1 BOTTLE (15631-2718-1)
Annotations
UNII (FDA Substance ID)
F1T8QT9U8B
DIGITALIS
RxCUI 91235
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F1T8QT9U8B",
"rxcui": "91235",
"inchikey": null,
"display_name": "DIGITALIS",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"19ba912f-cd86-4cca-e063-6294a90a233b": {
"match": "brand_token",
"title": "DIGITALIS PUR LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]",
"spl_version": "1",
"published_date": "2024-06-03"
}
},
"productid": "15631-2718_19ba75a8-51ad-c9f5-e063-6394a90a5214",
"productndc": "15631-2718",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIGITALIS",
"proprietary_name": "DIGITALIS PUR",
"active_ingred_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "DIGITALIS PUR",
"start_marketing_date": "20240523",
"active_numerator_strength": "6"
}Related drugs
Other records sharing ATC code C01AA03.
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