Package 54348-835-60

{"route": ["ORAL"], "spl_id": "eaa5cc60-19cc-a3f1-e053-2995a90a968f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["bb6d0547-c113-42f9-8bf2-c227a55ab758"], "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": ["PharmPak, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-00)  / 1 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-00", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-08)  / 8 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-08", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-10)  / 10 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-10", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-12)  / 12 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-12", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-20)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-20", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-30", "marketing_start_date": "20190711"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (54348-835-60)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54348-835-60", "marketing_start_date": "20190711"}], "brand_name": "Ibuprofen", "product_id": "54348-835_eaa5cc60-19cc-a3f1-e053-2995a90a968f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "54348-835", "generic_name": "IBUPROFEN", "labeler_name": "PharmPak, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20190711", "listing_expiration_date": "20261231"}