nabumetone

Generic: nabumetone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nabumetone
Generic Name nabumetone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

nabumetone 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-972
Product ID 43063-972_36c31358-008c-bd73-e063-6294a90a06cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078671
Listing Expiration 2026-12-31
Marketing Start 2019-03-06

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 43063972
Hyphenated Format 43063-972

Supplemental Identifiers

RxCUI
311892
UPC
0343063972205
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 ANDA078671 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)
source: ndc

Packages (2)

43063-972-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20) 43063-972-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)

Ingredients (1)

nabumetone (500 mg/1)

Linked Drug Pages (1)

Nabumetone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "36c31358-008c-bd73-e063-6294a90a06cf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0343063972205"], "unii": ["LW0TIW155Z"], "rxcui": ["311892"], "spl_set_id": ["8f3c1b1d-2765-4cb5-92df-044b99339c92"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)", "package_ndc": "43063-972-20", "marketing_start_date": "20190422"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)", "package_ndc": "43063-972-30", "marketing_start_date": "20190710"}], "brand_name": "Nabumetone", "product_id": "43063-972_36c31358-008c-bd73-e063-6294a90a06cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-972", "generic_name": "Nabumetone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "500 mg/1"}], "application_number": "ANDA078671", "marketing_category": "ANDA", "marketing_start_date": "20190306", "listing_expiration_date": "20261231"}