Package 41250-526-27

{"route": ["ORAL"], "spl_id": "57e4852c-fa51-410f-a9cd-e17c021ddca5", "openfda": {"unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["34d635f8-9703-4c29-92a5-85d3b47c4c93"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-526-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-526-27", "marketing_start_date": "20200121"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-526-60)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-526-60", "marketing_start_date": "20200114"}], "brand_name": "naproxen sodium pm", "product_id": "41250-526_57e4852c-fa51-410f-a9cd-e17c021ddca5", "dosage_form": "TABLET, FILM 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": "41250-526", "generic_name": "diphenhydramine hydrochloride, naproxen sodium", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium pm", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA208499", "marketing_category": "ANDA", "marketing_start_date": "20200114", "listing_expiration_date": "20261231"}