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United States · US · US:37662-2596_f3c363a2-8050-5c7f-e053-2a95a90aaebb
Granatum Punica
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766225961200 PELLET in 1 VIAL, GLASS (37662-2596-1)
- ndc113766225962500 PELLET in 1 VIAL, GLASS (37662-2596-2)
- ndc1137662259633000 PELLET in 1 BOTTLE, GLASS (37662-2596-3)
- ndc11376622596410000 PELLET in 1 BOTTLE, GLASS (37662-2596-4)
Annotations
UNII (FDA Substance ID)
CLV24I3T1D
PUNICA GRANATUM ROOT BARK
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "CLV24I3T1D",
"rxcui": null,
"inchikey": null,
"display_name": "PUNICA GRANATUM ROOT BARK",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"1f7cc316-9b47-1c93-e063-6394a90afd28": {
"match": "brand_token",
"title": "GRANATUM (PUNICA GRANATUM ROOT BARK) PELLET [BOIRON]",
"spl_version": "1",
"published_date": "2024-08-14"
}
},
"productid": "37662-2596_f3c363a2-8050-5c7f-e053-2a95a90aaebb",
"productndc": "37662-2596",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PUNICA GRANATUM ROOT BARK",
"proprietary_name": "Granatum Punica",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Granatum Punica",
"start_marketing_date": "20230202",
"active_numerator_strength": "200"
}Access this data programmatically
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