Package 63868-325-01

{"route": ["ORAL"], "spl_id": "2435717d-bbb9-9e00-e063-6394a90a75ad", "openfda": {"upc": ["0635515995970"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["475becec-1a56-4cfa-a0c5-562f8772adfb"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (63868-325-01)", "package_ndc": "63868-325-01", "marketing_end_date": "20261130", "marketing_start_date": "20071108"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-325-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-325-50", "marketing_end_date": "20261130", "marketing_start_date": "20071108"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "63868-325_2435717d-bbb9-9e00-e063-6394a90a75ad", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63868-325", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261130", "marketing_start_date": "20071108"}