Package 67751-241-01

{"route": ["ORAL"], "spl_id": "435b2b2a-6d47-1611-e063-6394a90a9f99", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["435b1a31-353d-af20-e063-6294a90aa907"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-241-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-241-01", "marketing_start_date": "20250311"}, {"sample": false, "description": "2 POUCH in 1 CARTON (67751-241-02)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-241-02", "marketing_start_date": "20250923"}], "brand_name": "Tylenol PM Extra Strength", "product_id": "67751-241_435b2b2a-6d47-1611-e063-6394a90a9f99", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-241", "generic_name": "acetaminophen and diphenhydramine hydrochloride", "labeler_name": "Navajo Manufacturing Company Inc.", "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": "20250311", "listing_expiration_date": "20261231"}