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United States · US · US:43063-972_36c31358-008c-bd73-e063-6294a90a06cf
Nabumetone
Orange BookUNIISPLATC M01AX01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeM01AX01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11430639722020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)
- ndc11430639723030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)
Annotations
UNII (FDA Substance ID)
LW0TIW155Z
NABUMETONE
RxCUI 31448
Orange Book
A078671
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": "43063-972_36c31358-008c-bd73-e063-6294a90a06cf",
"productndc": "43063-972",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "078671",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Mar 7, 2008"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "750MG",
"product_no": "002",
"approval_date": "Mar 7, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NABUMETONE",
"proprietary_name": "Nabumetone",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078671",
"marketing_category": "ANDA",
"nonproprietary_name": "Nabumetone",
"start_marketing_date": "20190306",
"active_numerator_strength": "500"
}Related drugs
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