Package 0591-3671-01
Brand: nabumetone
Generic: nabumetonePackage Facts
Identity
Package NDC
0591-3671-01
Digits Only
0591367101
Product NDC
0591-3671
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3671-01)
Marketing
Marketing Status
Brand
nabumetone
Generic
nabumetone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "50a45f4a-452a-43d5-8f93-38b1023dec1e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0305913670013"], "unii": ["LW0TIW155Z"], "rxcui": ["311892", "311893"], "spl_set_id": ["53656d70-6572-4669-6465-6c6973555341"], "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": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3671-01)", "package_ndc": "0591-3671-01", "marketing_start_date": "20110613"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3671-05)", "package_ndc": "0591-3671-05", "marketing_start_date": "20110613"}], "brand_name": "Nabumetone", "product_id": "0591-3671_50a45f4a-452a-43d5-8f93-38b1023dec1e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0591-3671", "generic_name": "Nabumetone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "750 mg/1"}], "application_number": "ANDA091083", "marketing_category": "ANDA", "marketing_start_date": "20110613", "listing_expiration_date": "20261231"}