Package 69396-172-01

{"route": ["ORAL"], "spl_id": "3729a3d5-0ccd-378f-e063-6294a90aa65c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0850058161327"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["37299475-e2f3-de26-e063-6394a90ad62d"], "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": ["Trifecta Pharmaceuticals USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (69396-172-01)", "package_ndc": "69396-172-01", "marketing_start_date": "20250609"}], "brand_name": "Ibuprofen", "product_id": "69396-172_3729a3d5-0ccd-378f-e063-6294a90aa65c", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69396-172", "generic_name": "Ibuprofen", "labeler_name": "Trifecta Pharmaceuticals USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA207095", "marketing_category": "ANDA", "marketing_start_date": "20230808", "listing_expiration_date": "20261231"}