Package 30142-278-80

{"route": ["ORAL"], "spl_id": "cc3a78e5-52f9-424b-ab27-1c4ab644c735", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0041260022029"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["15e649c4-d75f-e8c1-e063-6294a90a7747"], "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": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-278-80)  / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-278-80", "marketing_start_date": "20240507"}], "brand_name": "Ibuprofen PM", "product_id": "30142-278_cc3a78e5-52f9-424b-ab27-1c4ab644c735", "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": "30142-278", "generic_name": "Ibuprofen and Diphenhydramine Citrate", "labeler_name": "KROGER COMPANY", "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": "ANDA216204", "marketing_category": "ANDA", "marketing_start_date": "20240507", "listing_expiration_date": "20261231"}