Cuprum Carbonicum

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
3766205971
200 PELLET in 1 VIAL, GLASS (37662-0597-1)
ndc11
3766205972
500 PELLET in 1 VIAL, GLASS (37662-0597-2)
ndc11
3766205973
3000 PELLET in 1 BOTTLE, GLASS (37662-0597-3)
ndc11
3766205974
10000 PELLET in 1 BOTTLE, GLASS (37662-0597-4)

Annotations

UNII (FDA Substance ID)

GIK928GH0Y

BASIC CUPRIC CARBONATE

RxCUI 1313321

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "GIK928GH0Y",
    "rxcui": "1313321",
    "inchikey": "ZMMDPCMYTCRWFF-UHFFFAOYSA-J",
    "display_name": "BASIC CUPRIC CARBONATE",
    "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": "37662-0597_e1958178-cf2d-290a-e053-2995a90a926c",
  "productndc": "37662-0597",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BASIC CUPRIC CARBONATE",
  "proprietary_name": "Cuprum Carbonicum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Carbonicum",
  "start_marketing_date": "20220616",
  "active_numerator_strength": "100"
}

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