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United States · US · US:23155-763_09939351-6106-4b21-b923-1b034a6f8f1d
Lithium carbonate
Orange BookUNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc112315576301100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)
- ndc112315576305500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)
Annotations
UNII (FDA Substance ID)
2BMD2GNA4V
LITHIUM CARBONATE
RxCUI 42351
Orange Book
A205532
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": "23155-763_09939351-6106-4b21-b923-1b034a6f8f1d",
"productndc": "23155-763",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "205532",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "300MG",
"product_no": "001",
"approval_date": "Sep 29, 2016"
}
],
"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": "ANDA205532",
"marketing_category": "ANDA",
"nonproprietary_name": "Lithium carbonate",
"start_marketing_date": "20201020",
"active_numerator_strength": "300"
}Related drugs
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