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United States Β· US Β· US:37662-3039_fa47c370-d4b3-9d82-e053-6294a90a8551
Rubidium Fluoratum
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 4
- ndc11376623039180 PELLET in 1 VIAL, GLASS (37662-3039-1)
- ndc113766230392200 PELLET in 1 VIAL, GLASS (37662-3039-2)
- ndc1137662303931200 PELLET in 1 BOTTLE, GLASS (37662-3039-3)
- ndc1137662303944000 PELLET in 1 BOTTLE, GLASS (37662-3039-4)
Annotations
UNII (FDA Substance ID)
63564TNJ4R
RUBIDIUM FLUORIDE
RxCUI 1872046
Raw payload (JSON)
{
"unii": {
"unii": "63564TNJ4R",
"rxcui": "1872046",
"inchikey": "AHLATJUETSFVIM-UHFFFAOYSA-M",
"display_name": "RUBIDIUM FLUORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"productid": "37662-3039_fa47c370-d4b3-9d82-e053-6294a90a8551",
"productndc": "37662-3039",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "RUBIDIUM FLUORIDE",
"proprietary_name": "Rubidium Fluoratum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Rubidium Fluoratum",
"start_marketing_date": "20230427",
"active_numerator_strength": "30"
}Access this data programmatically
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