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United States · US · US:37662-2682_f450858c-a6d3-d5df-e053-2995a90ab1f7
Lithium Oxydatum
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
- ndc113766226821200 PELLET in 1 VIAL, GLASS (37662-2682-1)
- ndc113766226822500 PELLET in 1 VIAL, GLASS (37662-2682-2)
- ndc1137662268233000 PELLET in 1 BOTTLE, GLASS (37662-2682-3)
- ndc11376622682410000 PELLET in 1 BOTTLE, GLASS (37662-2682-4)
Annotations
UNII (FDA Substance ID)
2ON0O9YI0Q
LITHIUM OXIDE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2ON0O9YI0Q",
"rxcui": null,
"inchikey": "FUJCRWPEOMXPAD-UHFFFAOYSA-N",
"display_name": "LITHIUM OXIDE",
"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": "37662-2682_f450858c-a6d3-d5df-e053-2995a90ab1f7",
"productndc": "37662-2682",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LITHIUM OXIDE",
"proprietary_name": "Lithium Oxydatum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Lithium Oxydatum",
"start_marketing_date": "20230209",
"active_numerator_strength": "500"
}Related drugs
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