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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
- ndc11376621086180 PELLET in 1 VIAL, GLASS (37662-1086-1)
- ndc113766210862200 PELLET in 1 VIAL, GLASS (37662-1086-2)
- ndc1137662108631200 PELLET in 1 BOTTLE, GLASS (37662-1086-3)
- ndc1137662108644000 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"
}Access this data programmatically
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