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United States · US · US:37662-0823_e3a004d3-f771-e4e9-e053-2995a90ab43c
Digitalis Purpurea
UNIISPLATC C01AA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeC01AA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766208231200 PELLET in 1 VIAL, GLASS (37662-0823-1)
- ndc113766208232500 PELLET in 1 VIAL, GLASS (37662-0823-2)
- ndc1137662082333000 PELLET in 1 BOTTLE, GLASS (37662-0823-3)
- ndc11376620823410000 PELLET in 1 BOTTLE, GLASS (37662-0823-4)
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": "37662-0823_e3a004d3-f771-e4e9-e053-2995a90ab43c",
"productndc": "37662-0823",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIGITALIS",
"proprietary_name": "Digitalis Purpurea",
"active_ingred_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Digitalis Purpurea",
"start_marketing_date": "20220712",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code C01AA03.
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