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United States · US · US:37662-1086_e4e80242-9a46-5166-e053-2995a90a55e8

Cuprum Iodatum

UNIISPL

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

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
    3766210861
    80 PELLET in 1 VIAL, GLASS (37662-1086-1)
  • ndc11
    3766210862
    200 PELLET in 1 VIAL, GLASS (37662-1086-2)
  • ndc11
    3766210863
    1200 PELLET in 1 BOTTLE, GLASS (37662-1086-3)
  • ndc11
    3766210864
    4000 PELLET in 1 BOTTLE, GLASS (37662-1086-4)

Annotations

UNII (FDA Substance ID)
7DE9CA6IL2
CUPROUS IODIDE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7DE9CA6IL2",
    "rxcui": null,
    "inchikey": "LSXDOTMGLUJQCM-UHFFFAOYSA-M",
    "display_name": "CUPROUS IODIDE",
    "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": "37662-1086_e4e80242-9a46-5166-e053-2995a90a55e8",
  "productndc": "37662-1086",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CUPROUS IODIDE",
  "proprietary_name": "Cuprum Iodatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cuprum Iodatum",
  "start_marketing_date": "20220728",
  "active_numerator_strength": "30"
}

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