Cuprum Oxydatum Nigrum

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
3766206611
200 PELLET in 1 VIAL, GLASS (37662-0661-1)
ndc11
3766206612
500 PELLET in 1 VIAL, GLASS (37662-0661-2)
ndc11
3766206613
3000 PELLET in 1 BOTTLE, GLASS (37662-0661-3)
ndc11
3766206614
10000 PELLET in 1 BOTTLE, GLASS (37662-0661-4)

Annotations

UNII (FDA Substance ID)

V1XJQ704R4

CUPRIC OXIDE

RxCUI 21837

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "V1XJQ704R4",
    "rxcui": "21837",
    "inchikey": "KKCXRELNMOYFLS-UHFFFAOYSA-N",
    "display_name": "CUPRIC OXIDE",
    "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": "37662-0661_e1f8903e-f595-7cb3-e053-2a95a90ab08d",
  "productndc": "37662-0661",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPRIC OXIDE",
  "proprietary_name": "Cuprum Oxydatum Nigrum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Oxydatum Nigrum",
  "start_marketing_date": "20220621",
  "active_numerator_strength": "200"
}

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