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United States · US · US:37662-3175_fb747ef8-3ce0-317b-e053-6394a90a704a

Lithium Fluoratum

UNIISPLATC N05AN01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeN05AN01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    3766231751
    200 PELLET in 1 VIAL, GLASS (37662-3175-1)
  • ndc11
    3766231752
    500 PELLET in 1 VIAL, GLASS (37662-3175-2)
  • ndc11
    3766231753
    3000 PELLET in 1 BOTTLE, GLASS (37662-3175-3)
  • ndc11
    3766231754
    10000 PELLET in 1 BOTTLE, GLASS (37662-3175-4)

Annotations

UNII (FDA Substance ID)
1485XST65B
LITHIUM FLUORIDE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "1485XST65B",
    "rxcui": null,
    "inchikey": "PQXKHYXIUOZZFA-UHFFFAOYSA-M",
    "display_name": "LITHIUM FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "51b503f5-211f-a9cc-e063-6294a90a9895": {
      "match": "brand_token",
      "title": "LITHIUM CARBONATE ER (LITHIUM CARBONATE) TABLET [COUPLER LLC]",
      "spl_version": "1",
      "published_date": "2026-05-14"
    }
  },
  "productid": "37662-3175_fb747ef8-3ce0-317b-e053-6394a90a704a",
  "productndc": "37662-3175",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LITHIUM FLUORIDE",
  "proprietary_name": "Lithium Fluoratum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Lithium Fluoratum",
  "start_marketing_date": "20230516",
  "active_numerator_strength": "100"
}

Related drugs

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