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United States · US · US:70518-4627_5072144b-30c0-ed6a-e063-6394a90a2b9c
lithium carbonate
Orange BookUNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11705184627050 POUCH in 1 BOX (70518-4627-0) / 1 CAPSULE in 1 POUCH (70518-4627-1)
Annotations
UNII (FDA Substance ID)
2BMD2GNA4V
LITHIUM CARBONATE
RxCUI 42351
Orange Book
A090702
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": "70518-4627_5072144b-30c0-ed6a-e063-6394a90a2b9c",
"productndc": "70518-4627",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "090702",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "150MG",
"product_no": "001",
"approval_date": "Sep 25, 2009"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "300MG",
"product_no": "002",
"approval_date": "Sep 25, 2009"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "003",
"approval_date": "Sep 25, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LITHIUM CARBONATE",
"proprietary_name": "lithium carbonate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090702",
"marketing_category": "ANDA",
"nonproprietary_name": "lithium carbonate",
"start_marketing_date": "20260424",
"active_numerator_strength": "150"
}Related drugs
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