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United States · US · US:37662-3765_03389426-36db-99ad-e063-6394a90a8132
Lithium 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
- ndc113766237651200 PELLET in 1 VIAL, GLASS (37662-3765-1)
- ndc113766237652500 PELLET in 1 VIAL, GLASS (37662-3765-2)
- ndc1137662376533000 PELLET in 1 BOTTLE, GLASS (37662-3765-3)
- ndc11376623765410000 PELLET in 1 BOTTLE, GLASS (37662-3765-4)
Annotations
UNII (FDA Substance ID)
1685PBD1HF
LITHIUM IODATE
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "1685PBD1HF",
"rxcui": null,
"inchikey": "FZAXZVHFYFGNBX-UHFFFAOYSA-M",
"display_name": "LITHIUM IODATE",
"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": "37662-3765_03389426-36db-99ad-e063-6394a90a8132",
"productndc": "37662-3765",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LITHIUM IODATE",
"proprietary_name": "Lithium Iodatum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Lithium Iodatum",
"start_marketing_date": "20230818",
"active_numerator_strength": "200"
}Access this data programmatically
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