Beryllium Fluoratum

UNIISPL

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
6354544901
200 PELLET in 1 VIAL, GLASS (63545-449-01)
ndc11
6354544902
500 PELLET in 1 VIAL, GLASS (63545-449-02)
ndc11
6354544903
3000 PELLET in 1 BOTTLE, GLASS (63545-449-03)
ndc11
6354544904
10000 PELLET in 1 BOTTLE, GLASS (63545-449-04)

Annotations

UNII (FDA Substance ID)

499FU9DQ5C

BERYLLIUM FLUORIDE

RxCUI 2599581

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "499FU9DQ5C",
    "rxcui": "2599581",
    "inchikey": "JZKFIPKXQBZXMW-UHFFFAOYSA-L",
    "display_name": "BERYLLIUM FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "850136ef-8fcf-7c09-e053-2a91aa0a6abd": {
      "match": "brand_token",
      "title": "BERYLLIUM METALLICUM (BERYLLIUM) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2023-11-10"
    }
  },
  "productid": "63545-449_dd1b5fdf-b6a5-4040-e053-2a95a90aa761",
  "productndc": "63545-449",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BERYLLIUM FLUORIDE",
  "proprietary_name": "Beryllium Fluoratum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Beryllium Fluoratum",
  "start_marketing_date": "20220420",
  "active_numerator_strength": "200"
}

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