Package 72189-231-21

{"route": ["ORAL"], "spl_id": "2c285455-94b8-8154-e063-6394a90a0e8c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806", "197807"], "spl_set_id": ["c3f30813-0848-6e8a-e053-2995a90a3dea"], "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": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)", "package_ndc": "72189-231-21", "marketing_start_date": "20210604"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)", "package_ndc": "72189-231-30", "marketing_start_date": "20210604"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-231-60)", "package_ndc": "72189-231-60", "marketing_start_date": "20210604"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-231-90)", "package_ndc": "72189-231-90", "marketing_start_date": "20210604"}], "brand_name": "IBUPROFEN", "product_id": "72189-231_2c285455-94b8-8154-e063-6394a90a0e8c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-231", "generic_name": "IBUPROFEN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20210604", "listing_expiration_date": "20261231"}