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United States · US · US:64980-278_c2afa358-e66b-48aa-8c51-79b55ac31016
Lithium Carbonate
Orange BookUNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116498027801100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-278-01)
Annotations
UNII (FDA Substance ID)
2BMD2GNA4V
LITHIUM CARBONATE
RxCUI 42351
Orange Book
A205663
AB
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": "64980-278_c2afa358-e66b-48aa-8c51-79b55ac31016",
"productndc": "64980-278",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "205663",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "450MG",
"product_no": "001",
"approval_date": "Jun 5, 2017"
}
],
"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": "ANDA205663",
"marketing_category": "ANDA",
"nonproprietary_name": "Lithium Carbonate",
"start_marketing_date": "20180301",
"active_numerator_strength": "450"
}Related drugs
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