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United States · US · US:37662-2898_f82c4c19-c31c-55d8-e053-6294a90a9c3b

Cuprum Sulphuricum

UNIISPLATC V03AB20

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeV03AB20
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    3766228981
    200 PELLET in 1 VIAL, GLASS (37662-2898-1)
  • ndc11
    3766228982
    500 PELLET in 1 VIAL, GLASS (37662-2898-2)
  • ndc11
    3766228983
    3000 PELLET in 1 BOTTLE, GLASS (37662-2898-3)
  • ndc11
    3766228984
    10000 PELLET in 1 BOTTLE, GLASS (37662-2898-4)

Annotations

UNII (FDA Substance ID)
LRX7AJ16DT
CUPRIC SULFATE
RxCUI 21579
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "LRX7AJ16DT",
    "rxcui": "21579",
    "inchikey": "JZCCFEFSEZPSOG-UHFFFAOYSA-L",
    "display_name": "CUPRIC SULFATE",
    "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": "37662-2898_f82c4c19-c31c-55d8-e053-6294a90a9c3b",
  "productndc": "37662-2898",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPRIC SULFATE",
  "proprietary_name": "Cuprum Sulphuricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Sulphuricum",
  "start_marketing_date": "20230331",
  "active_numerator_strength": "200"
}

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