0591-3670

Generic: nabumetone

Labeler: actavis pharma, inc.
NDC Directory DRUG FOR FURTHER PROCESSING DRUG FOR FURTHER PROCESSING Active

Drug Facts

Product Profile

Brand Name
Generic Name nabumetone
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED
Active Ingredients

nabumetone 500 mg/1

Identifiers & Regulatory

Product NDC 0591-3670
Product ID 0591-3670_1d6f0d61-13ba-4154-8cc3-4e4c17c0ebcc
Product Type DRUG FOR FURTHER PROCESSING
Marketing Category DRUG FOR FURTHER PROCESSING
Listing Expiration 2026-12-31
Marketing Start 2011-06-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05913670
Hyphenated Format 0591-3670

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: label)
Generic Name nabumetone (source: ndc)
Application Number ANDA091083 (source: label)
Routes
oral
source: label

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 15150 TABLET, FILM COATED in 1 BOX (0591-3670-00)
  • 18180 TABLET, FILM COATED in 1 CONTAINER (0591-3670-77)
source: ndc

Packages (2)

0591-3670-00 15150 TABLET, FILM COATED in 1 BOX (0591-3670-00) 0591-3670-77 18180 TABLET, FILM COATED in 1 CONTAINER (0591-3670-77)

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 
{"spl_id": "1d6f0d61-13ba-4154-8cc3-4e4c17c0ebcc", "openfda": {}, "finished": false, "packaging": [{"description": "15150 TABLET, FILM COATED in 1 BOX (0591-3670-00)", "package_ndc": "0591-3670-00", "marketing_start_date": "13-JUN-11"}, {"description": "18180 TABLET, FILM COATED in 1 CONTAINER (0591-3670-77)", "package_ndc": "0591-3670-77", "marketing_start_date": "16-SEP-24"}], "product_id": "0591-3670_1d6f0d61-13ba-4154-8cc3-4e4c17c0ebcc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-3670", "generic_name": "Nabumetone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "NABUMETONE", "strength": "500 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20110613", "listing_expiration_date": "20261231"}