nabumetone

Generic: nabumetone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nabumetone
Generic Name nabumetone
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nabumetone 750 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6167
Product ID 50090-6167_ae902cbe-e8b4-42c9-8e85-828d7ca2d2f6
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 500906167
Hyphenated Format 50090-6167

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 (50090-6167-0)
  • 14 TABLET in 1 BOTTLE (50090-6167-2)
  • 60 TABLET in 1 BOTTLE (50090-6167-3)
  • 20 TABLET in 1 BOTTLE (50090-6167-4)
source: ndc

Packages (4)

Ingredients (1)

nabumetone (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ae902cbe-e8b4-42c9-8e85-828d7ca2d2f6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["LW0TIW155Z"], "rxcui": ["311893"], "spl_set_id": ["d997d125-dfc5-4cc5-b7a6-03f5a7248d14"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6167-0)", "package_ndc": "50090-6167-0", "marketing_start_date": "20221013"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-6167-2)", "package_ndc": "50090-6167-2", "marketing_start_date": "20221013"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6167-3)", "package_ndc": "50090-6167-3", "marketing_start_date": "20221013"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-6167-4)", "package_ndc": "50090-6167-4", "marketing_start_date": "20221013"}], "brand_name": "Nabumetone", "product_id": "50090-6167_ae902cbe-e8b4-42c9-8e85-828d7ca2d2f6", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-6167", "generic_name": "Nabumetone", "labeler_name": "A-S Medication Solutions", "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"}