Package 85509-1010-3

{"route": ["ORAL"], "spl_id": "39a9d46c-6833-d3cc-e063-6394a90adfe3", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["397f1f23-10c2-569e-e063-6394a90a7164"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1010-3)", "package_ndc": "85509-1010-3", "marketing_start_date": "20250721"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1010-6)", "package_ndc": "85509-1010-6", "marketing_start_date": "20250721"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-1010-9)", "package_ndc": "85509-1010-9", "marketing_start_date": "20250721"}], "brand_name": "Ibuprofen and famotidine", "product_id": "85509-1010_39a9d46c-6833-d3cc-e063-6394a90adfe3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-1010", "generic_name": "Ibuprofen and famotidine", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen and famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "26.6 mg/1"}, {"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA211890", "marketing_category": "ANDA", "marketing_start_date": "20210804", "listing_expiration_date": "20261231"}