nabumetone

Generic: nabumetone

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nabumetone
Generic Name nabumetone
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nabumetone 750 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0104
Product ID 80425-0104_2a99aae5-c902-7940-e063-6294a90a4146
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078420
Listing Expiration 2026-12-31
Marketing Start 2019-06-26

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250104
Hyphenated Format 80425-0104

Supplemental Identifiers

RxCUI
311893
UNII
LW0TIW155Z
NUI
N0000000160 M0001335 N0000175722

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nabumetone (source: ndc)
Generic Name nabumetone (source: ndc)
Application Number ANDA078420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80425-0104-1)
  • 60 TABLET in 1 BOTTLE (80425-0104-2)
  • 90 TABLET in 1 BOTTLE (80425-0104-3)
source: ndc

Packages (3)

Ingredients (1)

nabumetone (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99aae5-c902-7940-e063-6294a90a4146", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["LW0TIW155Z"], "rxcui": ["311893"], "spl_set_id": ["b43db4aa-6013-3942-e053-2a95a90a5189"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0104-1)", "package_ndc": "80425-0104-1", "marketing_start_date": "20190626"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0104-2)", "package_ndc": "80425-0104-2", "marketing_start_date": "20230407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0104-3)", "package_ndc": "80425-0104-3", "marketing_start_date": "20230407"}], "brand_name": "Nabumetone", "product_id": "80425-0104_2a99aae5-c902-7940-e063-6294a90a4146", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0104", "generic_name": "Nabumetone", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "750 mg/1"}], "application_number": "ANDA078420", "marketing_category": "ANDA", "marketing_start_date": "20190626", "listing_expiration_date": "20261231"}