Cuprum Phosphoricum

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
3766222311
80 PELLET in 1 VIAL, GLASS (37662-2231-1)
ndc11
3766222312
200 PELLET in 1 VIAL, GLASS (37662-2231-2)
ndc11
3766222313
1200 PELLET in 1 BOTTLE, GLASS (37662-2231-3)
ndc11
3766222314
4000 PELLET in 1 BOTTLE, GLASS (37662-2231-4)

Annotations

UNII (FDA Substance ID)

N8NP6FR80R

CUPRIC PHOSPHATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "N8NP6FR80R",
    "rxcui": null,
    "inchikey": "GQDHEYWVLBJKBA-UHFFFAOYSA-H",
    "display_name": "CUPRIC PHOSPHATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4b348c61-01cc-641a-e063-6294a90a53e7": {
      "match": "brand_token",
      "title": "CUPRUM METALLICUM LIQUID [NEWTON LABORATORIES, INC.]",
      "spl_version": "1",
      "published_date": "2026-02-23"
    }
  },
  "productid": "37662-2231_f166517a-76d5-cc19-e053-2995a90ae4f1",
  "productndc": "37662-2231",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPRIC PHOSPHATE",
  "proprietary_name": "Cuprum Phosphoricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Phosphoricum",
  "start_marketing_date": "20230103",
  "active_numerator_strength": "30"
}

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