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United States · US · US:0121-1027_bfaabf01-1b65-43db-839a-d1b66fafec18
Lithium
Orange BookUNIISPLATC N05AN01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPAI Holdings, LLC dba PAI Pharma
CountryUS (United States)
ATC codeN05AN01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110121102716500 mL in 1 BOTTLE (0121-1027-16)
Annotations
UNII (FDA Substance ID)
5Z6E9K79YV
LITHIUM CITRATE
RxCUI 52105
Orange Book
A070755
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5Z6E9K79YV",
"rxcui": "52105",
"inchikey": "HXGWMCJZLNWEBC-UHFFFAOYSA-K",
"display_name": "LITHIUM CITRATE",
"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": "0121-1027_bfaabf01-1b65-43db-839a-d1b66fafec18",
"productndc": "0121-1027",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "070755",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "EQ 300MG CARBONATE/5ML",
"product_no": "001",
"approval_date": "May 21, 1986"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LITHIUM CITRATE",
"proprietary_name": "Lithium",
"active_ingred_unit": "meq/5mL",
"application_number": "ANDA070755",
"marketing_category": "ANDA",
"nonproprietary_name": "Lithium",
"start_marketing_date": "20260414",
"active_numerator_strength": "8"
}Related drugs
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