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United States · US · US:37662-3758_03280bb4-794e-57bb-e063-6394a90a854f
Lithium Sulphuratum
UNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766237581200 PELLET in 1 VIAL, GLASS (37662-3758-1)
- ndc113766237582500 PELLET in 1 VIAL, GLASS (37662-3758-2)
- ndc1137662375833000 PELLET in 1 BOTTLE, GLASS (37662-3758-3)
- ndc11376623758410000 PELLET in 1 BOTTLE, GLASS (37662-3758-4)
Annotations
UNII (FDA Substance ID)
919XA137JK
LITHIUM SULFATE
RxCUI 28818
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "919XA137JK",
"rxcui": "28818",
"inchikey": "INHCSSUBVCNVSK-UHFFFAOYSA-L",
"display_name": "LITHIUM SULFATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"51b503f5-211f-a9cc-e063-6294a90a9895": {
"match": "brand_token",
"title": "LITHIUM CARBONATE ER (LITHIUM CARBONATE) TABLET [COUPLER LLC]",
"spl_version": "1",
"published_date": "2026-05-14"
}
},
"productid": "37662-3758_03280bb4-794e-57bb-e063-6394a90a854f",
"productndc": "37662-3758",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LITHIUM SULFATE",
"proprietary_name": "Lithium Sulphuratum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Lithium Sulphuratum",
"start_marketing_date": "20230817",
"active_numerator_strength": "500"
}Related drugs
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