Package 53209-1002-2

{"route": ["ORAL"], "spl_id": "37e8f74e-9c3f-b0e7-e063-6394a90a5106", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["6cd07a01-7034-4994-bbd3-bedcdf7d5b83"], "manufacturer_name": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 POUCH (53209-1002-2)  / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1002-1)", "package_ndc": "53209-1002-2", "marketing_start_date": "20250619"}], "brand_name": "Tylenol PM Extra Strength", "product_id": "53209-1002_37e8f74e-9c3f-b0e7-e063-6394a90a5106", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "53209-1002", "generic_name": "acetaminophen and diphenhydramine hydrochloride", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol 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_start_date": "20250619", "listing_expiration_date": "20261231"}