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United States · US · US:63187-307_9f61b1e1-ce31-45de-ab89-7ab579ee5878
Nabumetone
Orange BookUNIISPLATC M01AX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeM01AX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11631873073030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-307-30)
Annotations
UNII (FDA Substance ID)
LW0TIW155Z
NABUMETONE
RxCUI 31448
Orange Book
A091083
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "LW0TIW155Z",
"rxcui": "31448",
"inchikey": "BLXXJMDCKKHMKV-UHFFFAOYSA-N",
"display_name": "NABUMETONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"e87289f4-d4f9-4510-aaa5-51f8f8167658": {
"match": "brand_token",
"title": "NABUMETONE TABLET, FILM COATED [ANI PHARMACEUTICALS, INC.]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "63187-307_9f61b1e1-ce31-45de-ab89-7ab579ee5878",
"productndc": "63187-307",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "091083",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Jun 13, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "750MG",
"product_no": "002",
"approval_date": "Jun 13, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NABUMETONE",
"proprietary_name": "Nabumetone",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091083",
"marketing_category": "ANDA",
"nonproprietary_name": "Nabumetone",
"start_marketing_date": "20110613",
"active_numerator_strength": "750"
}Related drugs
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