Package 55681-401-03

{"route": ["ORAL"], "spl_id": "0ec9297f-febe-03a4-e063-6294a90ad14a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["f03958f8-aeae-edf0-e053-2a95a90a3e9e"], "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": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-401-03)", "package_ndc": "55681-401-03", "marketing_start_date": "20221130"}], "brand_name": "Ibuprofen", "product_id": "55681-401_0ec9297f-febe-03a4-e063-6294a90ad14a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55681-401", "generic_name": "Ibuprofen", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20221130", "listing_expiration_date": "20261231"}