Cuprum Muriaticum

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
3766206141
200 PELLET in 1 VIAL, GLASS (37662-0614-1)
ndc11
3766206142
500 PELLET in 1 VIAL, GLASS (37662-0614-2)
ndc11
3766206143
3000 PELLET in 1 BOTTLE, GLASS (37662-0614-3)
ndc11
3766206144
10000 PELLET in 1 BOTTLE, GLASS (37662-0614-4)

Annotations

UNII (FDA Substance ID)

P484053J2Y

CUPRIC CHLORIDE ANHYDROUS

RxCUI 150596

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "P484053J2Y",
    "rxcui": "150596",
    "inchikey": "ORTQZVOHEJQUHG-UHFFFAOYSA-L",
    "display_name": "CUPRIC CHLORIDE ANHYDROUS",
    "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": "37662-0614_e1a79248-ab58-07e0-e053-2a95a90a1623",
  "productndc": "37662-0614",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPRIC CHLORIDE ANHYDROUS",
  "proprietary_name": "Cuprum Muriaticum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Muriaticum",
  "start_marketing_date": "20220617",
  "active_numerator_strength": "200"
}

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