nabumetone 750 mg

Generic: nabumetone

Labeler: lgm pharma solutions, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nabumetone 750 mg
Generic Name nabumetone
Labeler lgm pharma solutions, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

nabumetone 750 mg/1

Manufacturer
LGM PHARMA SOLUTIONS, LLC

Identifiers & Regulatory

Product NDC 79739-7077
Product ID 79739-7077_cf52d275-4853-4576-832a-07630bb644dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203166
Listing Expiration 2026-12-31
Marketing Start 2019-09-04

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 797397077
Hyphenated Format 79739-7077

Supplemental Identifiers

RxCUI
311892 311893 427726
UNII
LW0TIW155Z
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 750 mg (source: ndc)
Generic Name nabumetone (source: ndc)
Application Number ANDA203166 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (79739-7077-1)
  • 500 TABLET, FILM COATED in 1 BOTTLE (79739-7077-5)
source: ndc

Packages (2)

79739-7077-1 100 TABLET, FILM COATED in 1 BOTTLE (79739-7077-1) 79739-7077-5 500 TABLET, FILM COATED in 1 BOTTLE (79739-7077-5)

Ingredients (1)

nabumetone (750 mg/1)

Linked Drug Pages (1)

Nabumetone 500 mg, Nabumetone 750 mg, Nabumetone 1000 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf52d275-4853-4576-832a-07630bb644dc", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["LW0TIW155Z"], "rxcui": ["311892", "311893", "427726"], "spl_set_id": ["ef7c3da8-797f-4ea9-8999-53509785a0f7"], "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": ["LGM PHARMA SOLUTIONS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (79739-7077-1)", "package_ndc": "79739-7077-1", "marketing_start_date": "20190904"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (79739-7077-5)", "package_ndc": "79739-7077-5", "marketing_start_date": "20190904"}], "brand_name": "Nabumetone 750 mg", "product_id": "79739-7077_cf52d275-4853-4576-832a-07630bb644dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79739-7077", "generic_name": "Nabumetone", "labeler_name": "LGM PHARMA SOLUTIONS, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone 750 mg", "active_ingredients": [{"name": "NABUMETONE", "strength": "750 mg/1"}], "application_number": "ANDA203166", "marketing_category": "ANDA", "marketing_start_date": "20190904", "listing_expiration_date": "20261231"}