Package 71205-978-55
Brand: nabumetone
Generic: nabumetonePackage Facts
Identity
Package NDC
71205-978-55
Digits Only
7120597855
Product NDC
71205-978
Description
500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)
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": "40ce485f-575c-4c51-8058-83b10a8ddac7", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205977306"], "unii": ["LW0TIW155Z"], "rxcui": ["311892", "311893"], "spl_set_id": ["7a1643bf-6627-4b12-8246-6acc40517cf2"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00)", "package_ndc": "71205-978-00", "marketing_start_date": "20200507"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71205-978-30)", "package_ndc": "71205-978-30", "marketing_start_date": "20200507"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)", "package_ndc": "71205-978-55", "marketing_start_date": "20200507"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-978-60)", "package_ndc": "71205-978-60", "marketing_start_date": "20200507"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72)", "package_ndc": "71205-978-72", "marketing_start_date": "20200507"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-978-90)", "package_ndc": "71205-978-90", "marketing_start_date": "20200507"}], "brand_name": "Nabumetone", "product_id": "71205-978_40ce485f-575c-4c51-8058-83b10a8ddac7", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-978", "generic_name": "Nabumetone", "labeler_name": "Proficient Rx LP", "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": "20190925", "listing_expiration_date": "20261231"}