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United States · US · US:66267-561_1fa711ca-cee6-fae5-e063-6294a90aa5d0
Lovastatin
Orange BookUNIISPLATC C10AA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC10AA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11662675613030 TABLET in 1 BOTTLE (66267-561-30)
- ndc11662675619090 TABLET in 1 BOTTLE (66267-561-90)
Annotations
UNII (FDA Substance ID)
9LHU78OQFD
LOVASTATIN
RxCUI 6472
Orange Book
A075991
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9LHU78OQFD",
"rxcui": "6472",
"inchikey": "PCZOHLXUXFIOCF-BXMDZJJMSA-N",
"display_name": "LOVASTATIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"f5f265a6-2aa5-4205-9159-40133ae93ac0": {
"match": "brand_token",
"title": "LOVASTATIN TABLET [BRYANT RANCH PREPACK]",
"spl_version": "8",
"published_date": "2026-06-01"
}
},
"productid": "66267-561_1fa711ca-cee6-fae5-e063-6294a90aa5d0",
"productndc": "66267-561",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075991",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "001",
"approval_date": "Jun 5, 2002"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "002",
"approval_date": "Jun 5, 2002"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "003",
"approval_date": "Jun 5, 2002"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LOVASTATIN",
"proprietary_name": "Lovastatin",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075991",
"marketing_category": "ANDA",
"nonproprietary_name": "Lovastatin",
"start_marketing_date": "20021125",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code C10AA02.
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