Package 71335-2293-1

Brand: nabumetone

Generic: nabumetone
NDC Package

Package Facts

Identity

Package NDC 71335-2293-1
Digits Only 7133522931
Product NDC 71335-2293
Product ID 71335-2293_f8114f08-825e-40c1-8364-950c5eb71288
Description

500 TABLET in 1 BOTTLE (71335-2293-1)

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand nabumetone
Generic nabumetone
Sample Package No

Linked Drug Pages (1)

Nabumetone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f8114f08-825e-40c1-8364-950c5eb71288", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["LW0TIW155Z"], "rxcui": ["311893"], "spl_set_id": ["5a66c21f-4f06-4fb8-98fa-e81949586afd"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2293-1)", "package_ndc": "71335-2293-1", "marketing_start_date": "20231201"}], "brand_name": "Nabumetone", "product_id": "71335-2293_f8114f08-825e-40c1-8364-950c5eb71288", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-2293", "generic_name": "Nabumetone", "labeler_name": "Bryant Ranch Prepack", "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"}