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United States Β· US Β· US:37662-2921_f8a19f14-edd5-d02c-e053-6394a90afc99
Erbium Sulphuricum
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 4
- ndc113766229211200 PELLET in 1 VIAL, GLASS (37662-2921-1)
- ndc113766229212500 PELLET in 1 VIAL, GLASS (37662-2921-2)
- ndc1137662292133000 PELLET in 1 BOTTLE, GLASS (37662-2921-3)
- ndc11376622921410000 PELLET in 1 BOTTLE, GLASS (37662-2921-4)
Annotations
UNII (FDA Substance ID)
76R3969825
ERBIUM SULFATE OCTAHYDRATE
RxCUI 2049335
Raw payload (JSON)
{
"unii": {
"unii": "76R3969825",
"rxcui": "2049335",
"inchikey": "SMNPRCXUVYGCAE-UHFFFAOYSA-H",
"display_name": "ERBIUM SULFATE OCTAHYDRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"productid": "37662-2921_f8a19f14-edd5-d02c-e053-6394a90afc99",
"productndc": "37662-2921",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ERBIUM SULFATE OCTAHYDRATE",
"proprietary_name": "Erbium Sulphuricum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Erbium Sulphuricum",
"start_marketing_date": "20230405",
"active_numerator_strength": "100"
}Access this data programmatically
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