Rubidium Iodatum

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766230331
200 PELLET in 1 VIAL, GLASS (37662-3033-1)
ndc11
3766230332
500 PELLET in 1 VIAL, GLASS (37662-3033-2)
ndc11
3766230333
3000 PELLET in 1 BOTTLE, GLASS (37662-3033-3)
ndc11
3766230334
10000 PELLET in 1 BOTTLE, GLASS (37662-3033-4)

Annotations

UNII (FDA Substance ID)

18CYW0VL2X

RUBIDIUM IODIDE

Raw payload (JSON)

{
  "unii": {
    "unii": "18CYW0VL2X",
    "rxcui": null,
    "inchikey": "WFUBYPSJBBQSOU-UHFFFAOYSA-M",
    "display_name": "RUBIDIUM IODIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "37662-3033_fa217e9f-581d-6c6d-e053-6394a90a0905",
  "productndc": "37662-3033",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RUBIDIUM IODIDE",
  "proprietary_name": "Rubidium Iodatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rubidium Iodatum",
  "start_marketing_date": "20230424",
  "active_numerator_strength": "200"
}

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