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United States · US · US:33342-422_61fb32e9-a690-4004-862b-fb4f98b0c04b
lurasidone hydrochloride
Orange BookUNIISPLATC N05AE05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMacleods Pharmaceuticals Limited
CountryUS (United States)
ATC codeN05AE05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11333424220730 TABLET, FILM COATED in 1 BOTTLE (33342-422-07)
- ndc11333424221090 TABLET, FILM COATED in 1 BOTTLE (33342-422-10)
Annotations
UNII (FDA Substance ID)
O0P4I5851I
LURASIDONE HYDROCHLORIDE
RxCUI 1040027
Orange Book
A212124
ABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "O0P4I5851I",
"rxcui": "1040027",
"inchikey": "NEKCRUIRPWNMLK-SCIYSFAVSA-N",
"display_name": "LURASIDONE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2b07a830-93ba-427a-95fc-5138a6309f1e": {
"match": "brand_token",
"title": "LURASIDONE HYDROCHLORIDE TABLET, FILM COATED [MACLEODS PHARMACEUTICALS LIMITED]",
"spl_version": "4",
"published_date": "2026-04-29"
}
},
"productid": "33342-422_61fb32e9-a690-4004-862b-fb4f98b0c04b",
"productndc": "33342-422",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "212124",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Jun 9, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "002",
"approval_date": "Jun 9, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "60MG",
"product_no": "003",
"approval_date": "Jun 9, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "80MG",
"product_no": "004",
"approval_date": "Jun 9, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "120MG",
"product_no": "005",
"approval_date": "Jun 9, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LURASIDONE HYDROCHLORIDE",
"proprietary_name": "lurasidone hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA212124",
"marketing_category": "ANDA",
"nonproprietary_name": "lurasidone hydrochloride",
"start_marketing_date": "20230609",
"active_numerator_strength": "80"
}Related drugs
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