Package 71921-181-50

{"route": ["ORAL"], "spl_id": "1f260910-03d9-fa2f-e063-6294a90ac0b9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371921182015"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["c1733fdb-5eed-2094-e053-2995a90a6c8e"], "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": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71921-181-01)", "package_ndc": "71921-181-01", "marketing_start_date": "20211021"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71921-181-50)", "package_ndc": "71921-181-50", "marketing_start_date": "20211021"}], "brand_name": "Ibuprofen", "product_id": "71921-181_1f260910-03d9-fa2f-e063-6294a90ac0b9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71921-181", "generic_name": "Ibuprofen", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA071268", "marketing_category": "ANDA", "marketing_start_date": "20211021", "listing_expiration_date": "20261231"}