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United States Β· US Β· US:37662-4030_0663cace-3517-e497-e063-6394a90a9c68

Rubidium Muriaticum

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

  • ndc11
    3766240301
    200 PELLET in 1 VIAL, GLASS (37662-4030-1)
  • ndc11
    3766240302
    500 PELLET in 1 VIAL, GLASS (37662-4030-2)
  • ndc11
    3766240303
    3000 PELLET in 1 BOTTLE, GLASS (37662-4030-3)
  • ndc11
    3766240304
    10000 PELLET in 1 BOTTLE, GLASS (37662-4030-4)

Annotations

UNII (FDA Substance ID)
N3SHC5273S
RUBIDIUM CHLORIDE
RxCUI 1367087
Raw payload (JSON)
{
  "unii": {
    "unii": "N3SHC5273S",
    "rxcui": "1367087",
    "inchikey": "FGDZQCVHDSGLHJ-UHFFFAOYSA-M",
    "display_name": "RUBIDIUM CHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "37662-4030_0663cace-3517-e497-e063-6394a90a9c68",
  "productndc": "37662-4030",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RUBIDIUM CHLORIDE",
  "proprietary_name": "Rubidium Muriaticum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rubidium Muriaticum",
  "start_marketing_date": "20230927",
  "active_numerator_strength": "1"
}

Access this data programmatically

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Rubidium Muriaticum (US) β€” Drug Database