Package 50844-257-15

{"route": ["ORAL"], "spl_id": "1e0c28ae-8b35-4738-925e-2f7a6cda24e1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0052548689971"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["0ef4913b-5dc3-45bc-9cef-58601f8d2a79"], "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": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50844-257-15)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50844-257-15", "marketing_start_date": "20190722"}], "brand_name": "Ibuprofen", "product_id": "50844-257_1e0c28ae-8b35-4738-925e-2f7a6cda24e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-257", "generic_name": "Ibuprofen", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "20190722", "listing_expiration_date": "20261231"}