Package 82804-227-60
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
82804-227-60
Digits Only
8280422760
Product NDC
82804-227
Description
60 TABLET, FILM COATED in 1 BOTTLE (82804-227-60)
Marketing
Marketing Status
Brand
ibuprofen
Generic
ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92779e5b-b4e6-47bf-8544-615f8683f530", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0382804227303"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["ab2f1a30-611b-41b6-9baf-6a82305da845"], "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": "15 TABLET, FILM COATED in 1 BOTTLE (82804-227-15)", "package_ndc": "82804-227-15", "marketing_start_date": "20260116"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (82804-227-20)", "package_ndc": "82804-227-20", "marketing_start_date": "20260303"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-227-30)", "package_ndc": "82804-227-30", "marketing_start_date": "20250714"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-227-60)", "package_ndc": "82804-227-60", "marketing_start_date": "20250812"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-227-90)", "package_ndc": "82804-227-90", "marketing_start_date": "20250903"}], "brand_name": "Ibuprofen", "product_id": "82804-227_92779e5b-b4e6-47bf-8544-615f8683f530", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82804-227", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20271231"}