Package 69607-1970-1

{"route": ["ORAL"], "spl_id": "53818277-b127-4271-9604-8015eacd6c99", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0811079036964"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["1e2feaf0-7fff-43d5-bcfe-9f2851bdc805"], "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": ["WR Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (69607-1970-1)  / 120 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "69607-1970-1", "marketing_start_date": "20250228"}], "brand_name": "Ibuprofen PM", "product_id": "69607-1970_53818277-b127-4271-9604-8015eacd6c99", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69607-1970", "generic_name": "Diphenhydramine Citrate, Ibuprofen", "labeler_name": "WR Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA211404", "marketing_category": "ANDA", "marketing_start_date": "20250228", "listing_expiration_date": "20261231"}