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United States · US · US:72789-173_40a77b87-bcf9-bcb1-e063-6294a90ad29a
Lithium Carbonate
Orange BookUNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117278917301100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-173-01)
Annotations
UNII (FDA Substance ID)
2BMD2GNA4V
LITHIUM CARBONATE
RxCUI 42351
Orange Book
N017812
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2BMD2GNA4V",
"rxcui": "42351",
"inchikey": "XGZVUEUWXADBQD-UHFFFAOYSA-L",
"display_name": "LITHIUM CARBONATE",
"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": "72789-173_40a77b87-bcf9-bcb1-e063-6294a90ad29a",
"productndc": "72789-173",
"dosage_form": "CAPSULE, GELATIN COATED",
"orange_book": {
"appl_no": "017812",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "300MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "150MG",
"product_no": "002",
"approval_date": "Jan 28, 1987"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "600MG",
"product_no": "003",
"approval_date": "Jan 28, 1987"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LITHIUM CARBONATE",
"proprietary_name": "Lithium Carbonate",
"active_ingred_unit": "mg/1",
"application_number": "NDA017812",
"marketing_category": "NDA",
"nonproprietary_name": "Lithium Carbonate",
"start_marketing_date": "19801126",
"active_numerator_strength": "300"
}Related drugs
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