🇺🇸
United States · US · US:59762-1005_754ad7cd-edf5-4792-890d-07f0e4324c07
Cabergoline
Orange BookUNIISPLATC G02CB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMylan Pharmaceuticals Inc.
CountryUS (United States)
ATC codeG02CB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1159762100518 TABLET in 1 BOTTLE (59762-1005-1)
Annotations
UNII (FDA Substance ID)
LL60K9J05T
CABERGOLINE
RxCUI 47579
Orange Book
N020664
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "LL60K9J05T",
"rxcui": "47579",
"inchikey": "KORNTPPJEAJQIU-KJXAQDMKSA-N",
"display_name": "CABERGOLINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c9f0b576-d5e5-4e3e-bb5c-3574d75d9907": {
"match": "brand_token",
"title": "CABERGOLINE TABLET [A-S MEDICATION SOLUTIONS]",
"spl_version": "10",
"published_date": "2026-03-20"
}
},
"productid": "59762-1005_754ad7cd-edf5-4792-890d-07f0e4324c07",
"productndc": "59762-1005",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "020664",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "001",
"approval_date": "Dec 23, 1996"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CABERGOLINE",
"proprietary_name": "Cabergoline",
"active_ingred_unit": "mg/1",
"application_number": "NDA020664",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "cabergoline",
"start_marketing_date": "20140922",
"active_numerator_strength": ".5"
}Related drugs
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