Package 36800-292-06

{"route": ["ORAL"], "spl_id": "2c7a2c8d-cf4e-432d-9fe0-870eaf5b9e75", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0036800495791"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["59a88ca7-eb37-46de-9134-a5a6d330bd49"], "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": ["Topco Associates, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (36800-292-06)", "package_ndc": "36800-292-06", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "36800-292_2c7a2c8d-cf4e-432d-9fe0-870eaf5b9e75", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "36800-292", "generic_name": "Ibuprofen", "labeler_name": "Topco Associates, LLC", "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": "19880524", "listing_expiration_date": "20261231"}